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<!--This XML file contains a snapshot of the data displayed on the VMD Product Information Database.  File created on:11/04/2026 19:01:20-->
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    <VMDProductNo>A014424</VMDProductNo>
    <Name>Ecozole 4% w/w Premix for Medicated Feeding Stuff</Name>
    <MAHolder>Chanelle Pharmaceuticals Manufacturing Ltd</MAHolder>
    <Distributors>&lt;span&gt;Eco Animal Health Ltd&lt;/span&gt;</Distributors>
    <VMNo> 08749/3072</VMNo>
    <DateOfIssue>1995-07-06</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Fenbendazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Premix for medicated feeding stuff</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_3095906.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3095887.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A002069</VMDProductNo>
    <Name>Ecozole 4% w/w Premix for Medicated Feeding Stuff</Name>
    <MAHolder>Chanelle Pharmaceuticals Manufacturing Ltd</MAHolder>
    <Distributors>&lt;span&gt;Eco Animal Health Ltd&lt;/span&gt;</Distributors>
    <VMNo> 08749/5109</VMNo>
    <DateOfIssue>1995-07-06</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Fenbendazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Premix for medicated feeding stuff</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_112850.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_584556.PDF</PAAR_Link>
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    <VMDProductNo>A013224</VMDProductNo>
    <Name>Milbeguard Duo 4 mg / 10 mg Film Coated Tablets for Small Cats and Kittens</Name>
    <MAHolder>Ceva Sante Animale</MAHolder>
    <Distributors>&lt;span&gt;Ceva Animal Health Limited&lt;/span&gt;</Distributors>
    <VMNo> 14966/3011</VMNo>
    <DateOfIssue>2023-11-02</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Film-coated tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2664891.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3029039.PDF</PAAR_Link>
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    <VMDProductNo>A009517</VMDProductNo>
    <Name>Coliprotec F4/F18 Lyophilisate for Oral Suspension </Name>
    <MAHolder>Elanco Europe Ltd</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd.&lt;/span&gt;</Distributors>
    <VMNo>00879/5000</VMNo>
    <DateOfIssue>2017-01-09</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Escherichia coli</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate for Oral Suspension</PharmaceuticalForm>
    <TherapeuticGroup>Live Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2285249.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2022328.PDF</PAAR_Link>
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    <VMDProductNo>A013050</VMDProductNo>
    <Name>AviPro AE Suspension for Use in Drinking Water for Chicken</Name>
    <MAHolder>Elanco Europe Ltd</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>00879/5005</VMNo>
    <DateOfIssue>2023-06-21</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Avian encephalomyelitis virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for use in drinking water</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2582212.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_2253267.PDF</UKPAR_Link>
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    <VMDProductNo>A013214</VMDProductNo>
    <Name>Elanco Milbemycin - Praziquantel 2.5 mg/25 mg Chewable Tablets for Small Dogs and Puppies</Name>
    <MAHolder>Elanco Europe Ltd</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
    <VMNo>00879/5006</VMNo>
    <DateOfIssue>2022-12-29</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2469561.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_2477398.PDF</UKPAR_Link>
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    <VMDProductNo>A013213</VMDProductNo>
    <Name>Elanco Milbemycin - Praziquantel 2.5 mg/25 mg Tablets for Small Dogs and Puppies</Name>
    <MAHolder>Elanco Europe Ltd</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
    <VMNo>00879/5007</VMNo>
    <DateOfIssue>2022-12-29</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2469573.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_2471736.PDF</UKPAR_Link>
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    <VMDProductNo>A013217</VMDProductNo>
    <Name>Elanco Milbemycin - Praziquantel 4 mg/10 mg Film-Coated Tablets for Small Cats and Kittens</Name>
    <MAHolder>Elanco Europe Ltd</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
    <VMNo>00879/5008</VMNo>
    <DateOfIssue>2022-12-29</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Coated tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2469593.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_2471748.PDF</UKPAR_Link>
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    <VMDProductNo>A013212</VMDProductNo>
    <Name>Elanco Milbemycin - Praziquantel 12.5 mg/125 mg Tablets for Dogs    </Name>
    <MAHolder>Elanco Europe Ltd</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
    <VMNo>00879/5009</VMNo>
    <DateOfIssue>2022-12-29</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2469322.PDF</SPC_Link>
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    <VMDProductNo>A013216</VMDProductNo>
    <Name>Elanco Milbemycin - Praziquantel 16 mg/40 mg Film-Coated Tablets for Cats</Name>
    <MAHolder>Elanco Europe Ltd</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Limited&lt;/span&gt;</Distributors>
    <VMNo>00879/5010</VMNo>
    <DateOfIssue>2022-12-29</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Coated tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2469521.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_2471748.PDF</UKPAR_Link>
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    <VMDProductNo>A013279</VMDProductNo>
    <Name>Elanco Milbemycin - Praziquantel 12.5 mg/125 mg Chewable Tablets for Dogs    </Name>
    <MAHolder>Elanco Europe Ltd.</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Limited&lt;/span&gt;</Distributors>
    <VMNo>00879/5022</VMNo>
    <DateOfIssue>2023-02-20</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2502663.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_2471736.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2520304.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A013537</VMDProductNo>
    <Name>DrySeal 2.6 g Intramammary Suspension for Cattle</Name>
    <MAHolder>Elanco Europe Ltd</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Limited&lt;/span&gt;</Distributors>
    <VMNo>00879/5038</VMNo>
    <DateOfIssue>2024-08-09</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Bismuth Subnitrate</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Intramammary suspension</PharmaceuticalForm>
    <TherapeuticGroup>Miscellaneous mechanical teat seal </TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2839935.PDF</SPC_Link>
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    <VMDProductNo>A013712</VMDProductNo>
    <Name>Lotimil Plus 56.25 mg/2.11 mg Chewable Tablets (1.4–2.8 kg)</Name>
    <MAHolder>Elanco Europe Ltd</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
    <VMNo>00879/5043</VMNo>
    <DateOfIssue>2024-11-18</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Lotilaner, Milbemycin Oxime (A3 and A4)</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
    <TherapeuticGroup>Endectocide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2897724.PDF</SPC_Link>
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    <Name>Lotimil Plus 112.5 mg/4.22 mg Chewable Tablets (&gt; 2.8–5.5 kg)</Name>
    <MAHolder>Elanco Europe Ltd</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
    <VMNo>00879/5044</VMNo>
    <DateOfIssue>2024-11-18</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Lotilaner, Milbemycin Oxime (A3 and A4)</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
    <TherapeuticGroup>Endectocide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2899212.PDF</SPC_Link>
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    <Name>Lotimil Plus 225 mg/8.44 mg Chewable Tablets (&gt; 5.5–11 kg)</Name>
    <MAHolder>Elanco Europe Ltd</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
    <VMNo>00879/5045</VMNo>
    <DateOfIssue>2024-11-18</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Lotilaner, Milbemycin Oxime (A3 and A4)</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
    <TherapeuticGroup />
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2899261.PDF</SPC_Link>
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    <Name>Lotimil Plus 450 mg/16.88 mg Chewable Tablets (&gt; 11–22 kg)</Name>
    <MAHolder>Elanco Europe Ltd</MAHolder>
    <Distributors />
    <VMNo>00879/5046</VMNo>
    <DateOfIssue>2024-11-18</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Lotilaner, Milbemycin Oxime (A3 and A4)</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
    <TherapeuticGroup>Endectocide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2899307.PDF</SPC_Link>
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    <VMDProductNo>A013716</VMDProductNo>
    <Name>Lotimil Plus 900 mg/33.75 mg Chewable Tablets (&gt; 22–45 kg)</Name>
    <MAHolder>Elanco Europe Ltd</MAHolder>
    <Distributors />
    <VMNo>00879/5047</VMNo>
    <DateOfIssue>2024-11-18</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Lotilaner, Milbemycin Oxime (A3 and A4)</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
    <TherapeuticGroup>Endectocide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2899343.PDF</SPC_Link>
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    <VMDProductNo>A013698</VMDProductNo>
    <Name>Lotimil 12 mg Chewable Tablets for Cats (0.5–2.0 kg)</Name>
    <MAHolder>Elanco Europe Ltd</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd.&lt;/span&gt;</Distributors>
    <VMNo>00879/5048</VMNo>
    <DateOfIssue>2024-11-29</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Lotilaner</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2956609.PDF</SPC_Link>
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    <VMDProductNo>A013699</VMDProductNo>
    <Name>Lotimil 48 mg Chewable Tablets for Cats (&gt;2.0–8.0 kg)</Name>
    <MAHolder>Elanco Europe Ltd</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
    <VMNo>00879/5049</VMNo>
    <DateOfIssue>2024-11-29</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Lotilaner</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2956658.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_2961375.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2998024.PDF</PAAR_Link>
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    <VMDProductNo>A013811</VMDProductNo>
    <Name>Beaphar Flea 11.4 mg Tablets for Cats</Name>
    <MAHolder>Elanco Europe Ltd</MAHolder>
    <Distributors>&lt;span&gt;Beaphar (UK) Ltd&lt;/span&gt;</Distributors>
    <VMNo>00879/5050</VMNo>
    <DateOfIssue>2025-02-07</DateOfIssue>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Maropitant</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antiemetic</TherapeuticGroup>
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    <MAHolder>KRKA, d.d., Novo mesto</MAHolder>
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    <DateOfIssue>2021-08-26</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Film-coated tablet</PharmaceuticalForm>
    <TherapeuticGroup>Endectocide</TherapeuticGroup>
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    <UKPAR_Link />
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Film-coated tablet</PharmaceuticalForm>
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    <MAHolder>KRKA, d.d., Novo mesto</MAHolder>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Film-coated tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <DateOfIssue>2019-04-09</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Film-coated tablet</PharmaceuticalForm>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Doxycycline Hyclate</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens, Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Powder for use in drinking water </PharmaceuticalForm>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
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    <DistributionCategory>NFA-VPS</DistributionCategory>
    <PharmaceuticalForm>Film-coated tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic anticestodal</TherapeuticGroup>
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    <Distributors>&lt;span&gt;Krka d.d., Novo Mesto&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Selamectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
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    <Name>Selehold 45 mg Spot-on Solution for Cats 2.6–7.5 kg</Name>
    <MAHolder>KRKA, d.d., Novo mesto</MAHolder>
    <Distributors>&lt;span&gt;Krka d.d., Novo Mesto&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Selamectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
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    <Distributors>&lt;span&gt;Krka d.d., Novo Mesto&lt;/span&gt;</Distributors>
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    <DateOfIssue>2018-11-15</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Selamectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
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    <Distributors>&lt;span&gt;Krka d.d., Novo Mesto&lt;/span&gt;</Distributors>
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    <DateOfIssue>2018-11-15</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Selamectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Endectocide</TherapeuticGroup>
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    <MAHolder>KRKA, d.d., Novo mesto</MAHolder>
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    <DateOfIssue>2018-11-15</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Selamectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Selamectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Selamectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
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    <Distributors>&lt;span&gt;Krka d.d., Novo Mesto&lt;/span&gt;</Distributors>
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    <DateOfIssue>2018-11-15</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Selamectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Endectocide</TherapeuticGroup>
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    <MAHolder>KRKA, d.d., Novo mesto</MAHolder>
    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
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    <DateOfIssue>2013-07-18</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Flubendazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens, Pigs</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Enrofloxacin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <Name>Enroxil 50 mg/ml Solution for Injection for Calves, Pigs and Dogs</Name>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
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    <ActiveSubstances>Enrofloxacin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Tiamulin Hydrogen Fumarate</ActiveSubstances>
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    <Territory>Northern Ireland</Territory>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
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    <Territory>Northern Ireland</Territory>
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    <Territory>Northern Ireland</Territory>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
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    <Territory>Northern Ireland</Territory>
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    <ControlledDrug>N</ControlledDrug>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Equine influenza virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <Name>Equilis Te Suspension for Injection for Horses</Name>
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    <ActiveSubstances>Clostridium tetani</ActiveSubstances>
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    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
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    <Distributors>&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <DateOfIssue>2017-08-18</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
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    <ActiveSubstances>Fluralaner</ActiveSubstances>
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    <Distributors>&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Cell-associated live recombinant turkey herpesvirus</ActiveSubstances>
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    <PharmaceuticalForm>Lyophilisate and solvent for suspension for injection</PharmaceuticalForm>
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    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
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    <Distributors>&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <Name>Porcilis Porcoli Diluvac Forte</Name>
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    <Distributors>&lt;span&gt;Virbac (UK) Limited&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National</AuthorisationRoute>
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    <ActiveSubstances>Salmon pancreas disease virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Viral Vaccine</TherapeuticGroup>
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    <Name>Numelvi 4.8 mg Tablets for Dogs</Name>
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    <ActiveSubstances>Atinvicitinib</ActiveSubstances>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
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    <Name>Numelvi 7.2 mg Tablets for Dogs</Name>
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    <Distributors>&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Atinvicitinib</ActiveSubstances>
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    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
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    <Name>Numelvi 21.6 mg Tablets for Dogs</Name>
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    <Distributors>&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Atinvicitinib</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
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    <Name>Numelvi 31.6 mg Tablets for Dogs</Name>
    <MAHolder>MSD Animal Health UK Limited</MAHolder>
    <Distributors>&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>01708/5137</VMNo>
    <DateOfIssue>2026-01-20</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Atinvicitinib</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <Name>Beaphar Ear Drops, Solution</Name>
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    <Distributors>&lt;span&gt;Sinclair Animal &amp; Household Care Ltd&lt;/span&gt;</Distributors>
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    <Territory>Great Britain</Territory>
    <ActiveSubstances>Piperonyl Butoxide, Pyrethrins</ActiveSubstances>
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    <DistributionCategory>AVM-GSL</DistributionCategory>
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    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <VMDProductNo>A006043</VMDProductNo>
    <Name>Johnson’s 4Fleas Shampoo for Dogs 1.05% w/v</Name>
    <MAHolder>Johnson's Veterinary Products Ltd</MAHolder>
    <Distributors />
    <VMNo>01759/5001</VMNo>
    <DateOfIssue>2003-08-06</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Permethrin (Cis:Trans 25:75)</ActiveSubstances>
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    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>AVM-GSL</DistributionCategory>
    <PharmaceuticalForm>Shampoo</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <VMDProductNo>A001507</VMDProductNo>
    <Name>Johnson's Anti Pest Insect Spray</Name>
    <MAHolder>Johnson's Veterinary Products Ltd</MAHolder>
    <Distributors>&lt;span&gt;Johnson's Veterinary Products Ltd&lt;/span&gt;</Distributors>
    <VMNo>01759/5002</VMNo>
    <DateOfIssue>1991-10-08</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Piperonyl Butoxide, Pyrethrum Extract 25%</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>AVM-GSL</DistributionCategory>
    <PharmaceuticalForm>Cutaneous spray, solution</PharmaceuticalForm>
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    <DateOfIssue>1991-04-22</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Piperonyl Butoxide, Pyrethrum Extract 25%</ActiveSubstances>
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    <TargetSpecies>Budgerigar, Cage Birds, Common canary, Pigeon (non-food producing)</TargetSpecies>
    <DistributionCategory>AVM-GSL</DistributionCategory>
    <PharmaceuticalForm>Cutaneous spray, solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <ActiveSubstances>Piperonyl Butoxide, Pyrethrum Extract 25%</ActiveSubstances>
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    <Name>Johnson's Diarrhoea Tablets</Name>
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    <ActiveSubstances>Bismuth Carbonate Anhydrous, Calcium Carbonate</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>AVM-GSL</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Gastrointestinal antidiarrhoeal</TherapeuticGroup>
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    <Name>Johnson's Dog Flea Shampoo</Name>
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    <ActiveSubstances>Piperonyl Butoxide, Pyrethrins</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>AVM-GSL</DistributionCategory>
    <PharmaceuticalForm>Shampoo</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <ActiveSubstances>Piperonyl Butoxide, Pyrethrum Extract 25%</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <PharmaceuticalForm>Cutaneous spray, solution</PharmaceuticalForm>
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    <VMDProductNo>A000544</VMDProductNo>
    <Name>Johnson's Ear Drops, Solution</Name>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Piperonyl Butoxide, Pyrethrins</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>AVM-GSL</DistributionCategory>
    <PharmaceuticalForm>Ear drops, solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <VMDProductNo>A004668</VMDProductNo>
    <Name>Johnson's Flea &amp; Tick Drops 742 mg for Puppies &amp; Small Dogs, Cutaneous Solution</Name>
    <MAHolder>Johnson's Veterinary Products Ltd</MAHolder>
    <Distributors />
    <VMNo>01759/5009</VMNo>
    <DateOfIssue>2000-04-11</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Permethrin (cis:trans 25:75)</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>AVM-GSL</DistributionCategory>
    <PharmaceuticalForm>Cutaneous solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A003284</VMDProductNo>
    <Name>Johnson's Insecticidal Flea &amp; Tick Drops 742 mg, Cutaneous Solution</Name>
    <MAHolder>Johnson's Veterinary Products Ltd</MAHolder>
    <Distributors />
    <VMNo>01759/5010</VMNo>
    <DateOfIssue>1998-11-10</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Permethrin (cis:trans 25:75)</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>AVM-GSL</DistributionCategory>
    <PharmaceuticalForm>Cutaneous solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <VMDProductNo>A001492</VMDProductNo>
    <Name>Johnson's Pigeon Insect Spray</Name>
    <MAHolder>Johnson's Veterinary Products Ltd</MAHolder>
    <Distributors />
    <VMNo>01759/5011</VMNo>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Piperonyl Butoxide, Pyrethrum Extract 25%</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>AVM-GSL</DistributionCategory>
    <PharmaceuticalForm>Cutaneous spray, solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A000543</VMDProductNo>
    <Name>Johnson's Scaly Lotion, Cutaneous Solution</Name>
    <MAHolder>Johnson's Veterinary Products Ltd</MAHolder>
    <Distributors />
    <VMNo>01759/5012</VMNo>
    <DateOfIssue>1992-02-18</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Piperonyl Butoxide, Pyrethrins</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Budgerigar, Cage Birds, Common canary</TargetSpecies>
    <DistributionCategory>AVM-GSL</DistributionCategory>
    <PharmaceuticalForm>Cutaneous solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <VMDProductNo>A000299</VMDProductNo>
    <Name>Clinidip L Concentrate 2.0% w/v Concentrate for Teat Dip or Teat Spray Solution</Name>
    <MAHolder>GEA Farm Technologies (UK) Ltd</MAHolder>
    <Distributors />
    <VMNo>01808/5000</VMNo>
    <DateOfIssue>1992-08-28</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Iodine</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Goats, Sheep</TargetSpecies>
    <DistributionCategory>AVM-GSL</DistributionCategory>
    <PharmaceuticalForm>Teat dip/spray solution</PharmaceuticalForm>
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    <VMDProductNo>A000312</VMDProductNo>
    <Name>Clinidip 2.5 % w/v Superconcentrate Concentrate for Teat Dip or Teat Spray Solution</Name>
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    <Distributors />
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    <AuthorisationRoute>National</AuthorisationRoute>
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    <ActiveSubstances>Iodine</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>AVM-GSL</DistributionCategory>
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    <Name>Luxspray 50V 0.5% w/v Teat Dip / Teat Spray, Solution - Ready to Use</Name>
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    <Distributors />
    <VMNo>01808/5002</VMNo>
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    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
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    <ActiveSubstances>Iodine</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>AVM-GSL</DistributionCategory>
    <PharmaceuticalForm>Teat dip/spray solution</PharmaceuticalForm>
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    <Name>Sensospray 70V 0.74% w/v Teat Dip / Teat Spray, Solution - Ready to Use</Name>
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    <Distributors />
    <VMNo>01808/5003</VMNo>
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    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Chlorhexidine Gluconate</ActiveSubstances>
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    <PharmaceuticalForm>Teat dip/spray solution</PharmaceuticalForm>
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    <Name>Silkidip 0.5% w/v Teat Dip/Teat Spray, Solution - Ready to Use</Name>
    <MAHolder>GEA Farm Technologies (UK) Ltd</MAHolder>
    <Distributors />
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>AVM-GSL</DistributionCategory>
    <PharmaceuticalForm>Teat dip/spray solution</PharmaceuticalForm>
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    <Name>Suredip 0.74% w/v Teat Dip/Teat Spray, Solution – Ready to Use</Name>
    <MAHolder>GEA Farm Technologies (UK) Ltd</MAHolder>
    <Distributors />
    <VMNo>01808/5005</VMNo>
    <DateOfIssue>1985-02-14</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Chlorhexidine Gluconate</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>AVM-GSL</DistributionCategory>
    <PharmaceuticalForm>Teat dip/spray solution</PharmaceuticalForm>
    <TherapeuticGroup>Antiseptic</TherapeuticGroup>
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    <VMDProductNo>A011597</VMDProductNo>
    <Name>Closamectin Solution for Injection for Cattle</Name>
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    <Distributors>&lt;span&gt;Norbrook Laboratories Limited&lt;/span&gt;</Distributors>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <Name>Noromectin 18.7 mg/g Oral Paste for Horses</Name>
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    <PharmaceuticalForm>Oral paste</PharmaceuticalForm>
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    <Name>Noroclav 50 mg Tablets for Dogs and Cats</Name>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
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    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <Name>Carprofen Norbrook 50 mg/ml Solution for Injection for Cattle </Name>
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    <Distributors>&lt;span&gt;Norbrook Laboratories Limited&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Amoxicillin, Clavulanic Acid</ActiveSubstances>
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    <Name>Colvasone 0.2% w/v Solution for Injection</Name>
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    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <Name>Noroclox DC 500 mg Intramammary Suspension</Name>
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    <ActiveSubstances>Boric Acid, Calcium</ActiveSubstances>
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    <ActiveSubstances>Amoxicillin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
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    <ControlledDrug>N</ControlledDrug>
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    <ControlledDrug>N</ControlledDrug>
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    <ControlledDrug>N</ControlledDrug>
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    <VMDProductNo>A001238</VMDProductNo>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Mineral</TherapeuticGroup>
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    <ActiveSubstances>Procaine Benzylpenicillin</ActiveSubstances>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
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    <Name>Levacide Pour-on Solution 20% w/v</Name>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <Name>Noromectin 0.5% w/v Pour-on Solution</Name>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Pour-on solution</PharmaceuticalForm>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
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    <Name>Noromectin 0.08% w/v Drench Oral Solution</Name>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral solution</PharmaceuticalForm>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Powder for oral solution</PharmaceuticalForm>
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    <ActiveSubstances>Porcine parvovirus 27a viral protein 2</ActiveSubstances>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Telmisartan</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
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    <AuthorisationRoute>National</AuthorisationRoute>
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    <ActiveSubstances>Telmisartan</ActiveSubstances>
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    <PharmaceuticalForm>Oral solution</PharmaceuticalForm>
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    <ActiveSubstances>Gamithromycin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Pigs, Sheep</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
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    <AuthorisationRoute>National</AuthorisationRoute>
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    <ActiveSubstances>Chondrogenic induced equine allogeneic peripheral blood-derived mesenchymal stem cells</ActiveSubstances>
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    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
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    <ActiveSubstances>Tenogenic primed equine allogeneic peripheral blood-derived mesenchymal stem cells (tpMSCs)</ActiveSubstances>
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    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
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    <AuthorisationRoute>National</AuthorisationRoute>
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    <ActiveSubstances>Insulin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
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    <Distributors />
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    <AuthorisationRoute>National</AuthorisationRoute>
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    <ActiveSubstances>Mycoplasma hyopneumoniae</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
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    <Name>Advocate 400 mg + 100 mg Spot-on Solution for Extra-Large Dogs (&gt; 25–40 kg)</Name>
    <MAHolder>Elanco Animal Health GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Animal Health GmbH&lt;/span&gt;</Distributors>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
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    <MAHolder>Elanco Animal Health GmbH</MAHolder>
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    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
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    <Name>Advocate 40 mg + 4 mg Spot-on Solution for Small Cats (≤ 4 kg) and Ferrets</Name>
    <MAHolder>Elanco Animal Health GmbH</MAHolder>
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    <DateOfIssue>2003-04-02</DateOfIssue>
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    <DistributionCategory>POM-V</DistributionCategory>
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    <Name>Advocate 40 mg + 10 mg Spot-on Solution for Small Dogs (≤ 4 kg)</Name>
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    <DateOfIssue>2003-04-02</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
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    <ActiveSubstances>Imidacloprid, Moxidectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
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    <Name>Baycox Iron 36.4 + 182 mg/ml Suspension for Injection for Pigs</Name>
    <MAHolder>Elanco Animal Health GmbH</MAHolder>
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    <VMNo>04895/5006</VMNo>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
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    <Distributors>&lt;span&gt;Elanco Animal Health GmbH&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Pradofloxacin</ActiveSubstances>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
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    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <MAHolder>Virbac</MAHolder>
    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
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    <ControlledDrug>N</ControlledDrug>
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    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <Name>Fipronil Spot-on Solution by Virbac 402 mg for Very Large Dogs</Name>
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    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Fipronil</ActiveSubstances>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
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    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate for suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral and Inactivated Bacterial Vaccine</TherapeuticGroup>
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    <Distributors>&lt;span&gt;Virbac Limited&lt;/span&gt;</Distributors>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
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    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
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    <Distributors>&lt;span&gt;Virbac Limited&lt;/span&gt;</Distributors>
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    <DateOfIssue>2024-06-17</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
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    <Name>Milpro Chewy 25.0 mg / 250.0 mg Chewable Tablets for Large Dogs </Name>
    <MAHolder>VIRBAC</MAHolder>
    <Distributors>&lt;span&gt;Virbac Limited&lt;/span&gt;</Distributors>
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    <DateOfIssue>2024-06-17</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <Name>Vetflurane 1000 mg/g Inhalation Vapour, Liquid</Name>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Isoflurane</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Chinchilla, Dogs, Ferrets, Gerbil, Guinea Pig, Hamster, Horses, Mouse, Ornamental Birds, Rat, Reptiles</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Inhalation vapour, liquid</PharmaceuticalForm>
    <TherapeuticGroup>Neurological Agent general anaesthetic</TherapeuticGroup>
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    <Name>Ivermectin and Clorsulon 10 mg/ml / 100 mg/ml Solution for Injection for Cattle Virbac</Name>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Clorsulon, Ivermectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <Name>Canixin L Suspension for Injection for Dogs </Name>
    <MAHolder>Virbac</MAHolder>
    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
    <VMNo>05653/3029</VMNo>
    <DateOfIssue>2017-04-03</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Leptospira canicola, Leptospira icterohaemorrhagiae</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2741142.PDF</SPC_Link>
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    <Name>Virbamec Pour-on Solution for Cattle 5 mg/ml</Name>
    <MAHolder>Virbac</MAHolder>
    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Ivermectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Pour-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Endectocide</TherapeuticGroup>
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    <VMDProductNo>A011721</VMDProductNo>
    <Name>Effipro 2.5 mg/ml Cutaneous Spray, Solution for Cats and Dogs</Name>
    <MAHolder>Virbac</MAHolder>
    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
    <VMNo>05653/3031</VMNo>
    <DateOfIssue>2009-05-01</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Fipronil</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Cutaneous spray, solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <Name>Virbagest 4 mg/ml Oral Solution for Pigs</Name>
    <MAHolder>Virbac</MAHolder>
    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Altrenogest</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Oral solution</PharmaceuticalForm>
    <TherapeuticGroup>Hormone sex</TherapeuticGroup>
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    <MAHolder>VIRBAC</MAHolder>
    <Distributors>&lt;span&gt;Virbac&lt;/span&gt;</Distributors>
    <VMNo>05653/3033</VMNo>
    <DateOfIssue>2025-02-26</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Benazepril</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Premix for medicated feeding stuff</PharmaceuticalForm>
    <TherapeuticGroup>Cardio Vascular ACE inhibitor</TherapeuticGroup>
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    <MAHolder>Virbac</MAHolder>
    <Distributors>&lt;span&gt;Virbac Limited&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <Name>Effitix 67 mg/600 mg Spot-on Solution for Small Dogs</Name>
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    <ActiveSubstances>Fipronil, Permethrin (Cis:Trans 40:60)</ActiveSubstances>
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    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Deltamethrin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <PharmaceuticalForm>Pour-on solution</PharmaceuticalForm>
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    <Name>Zoletil 100 (50 mg/ml+50 mg/ml) Lyophilisate and Solvent for Solution for Injection for Dogs and Cats</Name>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate and solvent for solution for injection</PharmaceuticalForm>
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    <Name>Milpro 16 mg/40 mg Film-coated Tablets for Cats</Name>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Film-coated tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <Name>Tramvetol 50 mg Tablets for Dogs </Name>
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    <Distributors>&lt;span&gt;Virbac (UK) Limited&lt;/span&gt;</Distributors>
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    <Territory>Northern Ireland</Territory>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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  <CurrentAuthorisedProducts>
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    <Territory>Great Britain</Territory>
    <ActiveSubstances>Isoflurane</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Chinchilla, Dogs, Ferrets, Gerbil, Guinea Pig, Hamster, Horses, Mouse, Ornamental Birds, Rat, Reptiles</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Inhalation vapour, liquid</PharmaceuticalForm>
    <TherapeuticGroup>Neurological Agent general anaesthetic</TherapeuticGroup>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Clorsulon, Ivermectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Endectocide</TherapeuticGroup>
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    <DateOfIssue>2017-04-03</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Leptospira canicola, Leptospira icterohaemorrhagiae</ActiveSubstances>
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    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
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    <Territory>Great Britain</Territory>
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    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Pour-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Endectocide</TherapeuticGroup>
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    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Fipronil</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Cutaneous spray, solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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  <CurrentAuthorisedProducts>
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    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Altrenogest</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Oral solution</PharmaceuticalForm>
    <TherapeuticGroup>Hormone sex</TherapeuticGroup>
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    <Name>Benamix 6.25 mg/g Premix for Medicated Feeding Stuff for Cats </Name>
    <MAHolder>VIRBAC</MAHolder>
    <Distributors>&lt;span&gt;Virbac&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Benazepril</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Premix for medicated feeding stuff</PharmaceuticalForm>
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  <CurrentAuthorisedProducts>
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    <Name>Milpro 2.5 mg/25 mg Film-coated Tablets for Small Dogs and Puppies</Name>
    <MAHolder>Virbac</MAHolder>
    <Distributors>&lt;span&gt;Virbac Limited&lt;/span&gt;</Distributors>
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    <DateOfIssue>2014-07-15</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A008791</VMDProductNo>
    <Name>Milpro 12.5 mg/125 mg Film-coated Tablets for Dogs</Name>
    <MAHolder>VIRBAC</MAHolder>
    <Distributors>&lt;span&gt;Virbac Limited&lt;/span&gt;</Distributors>
    <VMNo>05653/5066</VMNo>
    <DateOfIssue>2014-07-15</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <VMDProductNo>A005876</VMDProductNo>
    <Name>Stabox 50% w/w Powder for Oral Solution for Pigs</Name>
    <MAHolder>Virbac</MAHolder>
    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
    <VMNo>05653/5067</VMNo>
    <DateOfIssue>2003-07-28</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Amoxicillin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Powder for oral solution</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
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    <Name>Thiamavance 10 mg/ml Oral Solution for Cats </Name>
    <MAHolder>VIRBAC</MAHolder>
    <Distributors>&lt;span&gt;Virbac&lt;/span&gt;</Distributors>
    <VMNo>05653/5068</VMNo>
    <DateOfIssue>2025-11-26</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Thiamazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Oral solution</PharmaceuticalForm>
    <TherapeuticGroup>Anti Hormone Agent</TherapeuticGroup>
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    <Name>Effitix 134 mg/1200 mg Spot-on Solution for Medium Dogs</Name>
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    <Distributors>&lt;span&gt;Virbac (UK) Limited&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Fipronil, Permethrin (Cis:Trans 40:60)</ActiveSubstances>
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    <DistributionCategory>POM-V</DistributionCategory>
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    <Distributors>&lt;span&gt;Virbac (UK) Limited&lt;/span&gt;</Distributors>
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    <MAHolder>Virbac</MAHolder>
    <Distributors>&lt;span&gt;Virbac (UK) Limited.&lt;/span&gt;</Distributors>
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    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
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    <VMDProductNo>A008053</VMDProductNo>
    <Name>Florfenikel 300 mg/ml Solution for Injection for Cattle and Pigs </Name>
    <MAHolder>Kela nv</MAHolder>
    <Distributors>&lt;span&gt;ANUPCO Limited&lt;/span&gt;</Distributors>
    <VMNo>06126/4001</VMNo>
    <DateOfIssue>2012-02-27</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Florfenicol</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A008533</VMDProductNo>
    <Name>Cefokel 50 mg/ml, Suspension for Injection for Pigs and Cattle </Name>
    <MAHolder>Kela – Kempisch Laboratorium – Kela Laboratoria nv</MAHolder>
    <Distributors>&lt;span&gt;ANUPCO Limited&lt;/span&gt;</Distributors>
    <VMNo>06126/4007</VMNo>
    <DateOfIssue>2013-05-23</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Ceftiofur</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A007960</VMDProductNo>
    <Name>Kelaprofen 100 mg/ml Solution for Injection for Cattle, Horses and Pigs</Name>
    <MAHolder>Kela – Kempisch Laboratorium – Kela Laboratoria nv</MAHolder>
    <Distributors>&lt;span&gt;ANUPCO Limited&lt;/span&gt;</Distributors>
    <VMNo>06126/5000</VMNo>
    <DateOfIssue>2012-02-27</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Ketoprofen</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Horses, Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Anti Inflammatory NSAID</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2329240.PDF</SPC_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012414</VMDProductNo>
    <Name>Resflor 300/16.5 mg/ml Solution for Injection for Cattle</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3002</VMNo>
    <DateOfIssue>2006-10-19</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Florfenicol, Flunixin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial; Anti Inflammatory</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2411532.PDF</SPC_Link>
    <UKPAR_Link />
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  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A011571</VMDProductNo>
    <Name>Chronogest CR, 20 mg Controlled Release Vaginal Sponge for Sheep</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3003</VMNo>
    <DateOfIssue>2005-06-21</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Flugestone Acetate</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Sheep</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Vaginal sponge</PharmaceuticalForm>
    <TherapeuticGroup>Hormone sex</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2539259.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2539309.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012071</VMDProductNo>
    <Name>Mastiplan LC, 300 mg/20 mg (Cefapirin/Prednisolone), Intramammary Suspension for Lactating Cows </Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3004</VMNo>
    <DateOfIssue>2007-05-25</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Cefapirin, Prednisolone</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Intramammary suspension</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial intramammary; Anti Inflammatory</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2381335.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2381353.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012481</VMDProductNo>
    <Name>Slice 2 mg/g Premix for Medicated Feeding Stuff</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3005</VMNo>
    <DateOfIssue>2000-01-13</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Emamectin Benzoate</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Atlantic salmon</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Premix for medicated feeding stuff</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2575105.PDF</SPC_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012305</VMDProductNo>
    <Name>Porcilis Lawsonia ID Lyophilisate and Solvent for Emulsion for Injection for Pigs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Ltd&lt;/span&gt;</Distributors>
    <VMNo>06376/3006</VMNo>
    <DateOfIssue>2020-12-23</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Lawsonia intracellularis</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate and solvent for emulsion for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2369480.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_1975077.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2502032.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A012307</VMDProductNo>
    <Name>Porcilis M Hyo ID Once Emulsion for Injection for Pigs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3007</VMNo>
    <DateOfIssue>2012-01-24</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Mycoplasma hyopneumoniae</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Emulsion for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2376380.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2376393.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A011462</VMDProductNo>
    <Name>Bovilis IBR Marker Inac Suspension for Injection for Cattle</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3008</VMNo>
    <DateOfIssue>2006-07-19</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Infectious bovine rhinotraceitis virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_159148.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2635611.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A012173</VMDProductNo>
    <Name>Nobilis RT + IBmulti + ND + EDS</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3009</VMNo>
    <DateOfIssue>2004-10-22</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Avian pneumovirus, Egg drop syndrome virus, Infectious bronchitis virus, Newcastle disease virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Emulsion for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2433493.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2433507.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A012303</VMDProductNo>
    <Name>Porcilis Ery+Parvo+Lepto Suspension for Injection for Pigs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3010</VMNo>
    <DateOfIssue>2016-12-22</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Erysipelothrix rhusiopathiae, Leptospira australis, Leptospira canicola, Leptospira grippotyphosa, Leptospira icterohaemorrhagiae, Leptospira pomona, Leptospira tarassovi, Porcine parvovirus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Viral and Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2467997.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_1989938.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2468048.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A012166</VMDProductNo>
    <Name>Nobilis E.coli inac Emulsion for Injection for Chickens</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3011</VMNo>
    <DateOfIssue>1994-12-30</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Escherichia coli</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Emulsion for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2564603.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2564615.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A012172</VMDProductNo>
    <Name>Nobilis RT + IBmulti + G + ND</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3012</VMNo>
    <DateOfIssue>2000-04-27</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Avian pneumovirus, Infectious bronchitis virus, Infectious bursal disease virus, Newcastle disease virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Emulsion for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2620395.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2620411.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A012180</VMDProductNo>
    <Name>Nobivac Ducat</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3013</VMNo>
    <DateOfIssue>2004-10-18</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Feline calicivirus, Feline viral rhinotracheitis virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate for suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_169140.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_557840.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A012181</VMDProductNo>
    <Name>Nobivac KC Nasal Drops, Lyophilisate and Solvent for Suspension for Dogs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3014</VMNo>
    <DateOfIssue>1999-11-15</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Bordetella bronchiseptica, Canine parainfluenza virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Nasal drops, lyophilisate and solvent for suspension</PharmaceuticalForm>
    <TherapeuticGroup>Live Bacterial and Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2580823.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_451183.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2580833.PDF</PAAR_Link>
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    <VMDProductNo>A012185</VMDProductNo>
    <Name>Nobivac Tricat Trio, Lyophilisate and Solvent for Suspension for Injection for Cats</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3015</VMNo>
    <DateOfIssue>2007-05-01</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Feline calicivirus, Feline panleukopenia virus, Feline viral rhinotracheitis virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate and solvent for suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_176445.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_261281.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012175</VMDProductNo>
    <Name>Nobilis Salenvac ETC Suspension for Injection for Chickens</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3016</VMNo>
    <DateOfIssue>2020-05-18</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Salmonella enteritidis, Salmonella Infantis, Salmonella typhimurium</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2362431.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_1928630.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2362454.PDF</PAAR_Link>
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    <VMDProductNo>A012306</VMDProductNo>
    <Name>Porcilis Lawsonia Lyophilisate and Solvent for Emulsion for Injection for Pigs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3017</VMNo>
    <DateOfIssue>2019-11-04</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Lawsonia intracellularis</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate and solvent for emulsion for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
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    <VMDProductNo>A011460</VMDProductNo>
    <Name>Bovilis Bovivac S</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3018</VMNo>
    <DateOfIssue>1999-08-10</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Salmonella dublin, Salmonella typhimurium</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
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    <VMDProductNo>A011743</VMDProductNo>
    <Name>Engemycin Spray, 25 mg/ml, Cutaneous Spray, Suspension for Cattle, Sheep and Pigs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3019</VMNo>
    <DateOfIssue>2009-10-13</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Oxytetracycline Hydrochloride</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Pigs, Sheep</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Cutaneous spray, suspension</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
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  </CurrentAuthorisedProducts>
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    <VMDProductNo>A011978</VMDProductNo>
    <Name>Heptavac P Plus Suspension for Injection for Sheep</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3020</VMNo>
    <DateOfIssue>1997-06-11</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Clostridium chauvoei, Clostridium novyi, Clostridium perfringens, Clostridium septicum, Clostridium tetani, Mannheimia haemolytica, Pasteurella trehalosi</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Sheep</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2593261.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2619390.PDF</PAAR_Link>
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    <VMDProductNo>A011463</VMDProductNo>
    <Name>Bovilis IBR Marker Live, Lyophilisate and Solvent for Suspension for Cattle</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3022</VMNo>
    <DateOfIssue>2002-02-13</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Infectious bovine rhinotraceitis virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Nasal drops, suspension</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2606862.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2606867.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A012183</VMDProductNo>
    <Name>Nobivac Respira Bb Suspension for Injection for Dogs </Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3023</VMNo>
    <DateOfIssue>2020-08-14</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Bordetella bronchiseptica</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2338574.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2338608.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A012184</VMDProductNo>
    <Name>Nobivac Respira Bb Suspension for Injection in Pre-filled Syringe for Dogs </Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3024</VMNo>
    <DateOfIssue>2020-08-18</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Bordetella bronchiseptica</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2338633.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2338656.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A011464</VMDProductNo>
    <Name>Bovilis INtranasal RSP Live, Nasal Spray, Lyophilisate and Solvent for Suspension for Cattle</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3025</VMNo>
    <DateOfIssue>2019-06-20</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Bovine parainfluenza virus 3, Bovine respiratory syncytial virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Nasal spray, lyophilisate for suspension</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2646078.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_1764158.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2646095.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A011461</VMDProductNo>
    <Name>Bovilis BVD Suspension for Injection for Cattle</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3026</VMNo>
    <DateOfIssue>1999-06-25</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Bovine viral diarrhoea virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2670879.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2670886.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012309</VMDProductNo>
    <Name>Porcilis PRRS Lyophilisate and Solvent for Suspension for Injection for Pigs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3027</VMNo>
    <DateOfIssue>2000-09-21</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Porcine respiratory and reproductive syndrome virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate for suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2385475.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2385493.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A011459</VMDProductNo>
    <Name>Bovilis Bovipast RSP</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3028</VMNo>
    <DateOfIssue>1999-06-25</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Bovine parainfluenza virus 3, Bovine respiratory syncytial virus, Mannheimia haemolytica</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Viral and Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2433295.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_464463.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2527075.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A010724</VMDProductNo>
    <Name>CepraShort 300 mg Intramammary Suspension for Dairy Cows at Drying-Off</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;</Distributors>
    <VMNo>06376/3029</VMNo>
    <DateOfIssue>2022-01-26</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Cefapirin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Intramammary suspension</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial intramammary</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2259154.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2891388.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012302</VMDProductNo>
    <Name>Porcilis APP Suspension for Injection</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3030</VMNo>
    <DateOfIssue>2014-02-11</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Actinobacillus pleuropneumoniae</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_561993.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_1989927.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_738917.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A012778</VMDProductNo>
    <Name>Bravoxin Suspension for Injection for Cattle and Sheep </Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd.&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3031</VMNo>
    <DateOfIssue>2021-03-05</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Clostridium chauvoei, Clostridium haemolyticum, Clostridium novyi, Clostridium perfringens, Clostridium septicum, Clostridium sordellii, Clostridium tetani</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Sheep</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2592901.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2592915.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A012170</VMDProductNo>
    <Name>Nobilis Paramyxo P201 emulsion for injection for pigeons</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd.&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3032</VMNo>
    <DateOfIssue>2002-10-10</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Pigeon paramyxo virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigeon (non-food producing)</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Emulsion for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2607067.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2607083.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A012235</VMDProductNo>
    <Name>Paracox-5, Suspension for Oral Suspension for Chickens</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3033</VMNo>
    <DateOfIssue>1999-06-28</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Eimeria acervulina, Eimeria maxima, Eimeria mitis, Eimeria tenella</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
    <TherapeuticGroup>Live Parasitic Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2605272.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_156251.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2605292.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A011465</VMDProductNo>
    <Name>Bovilis Rotavec Corona Emulsion for Injection for Cattle</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd.&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3034</VMNo>
    <DateOfIssue>2000-03-16</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Bovine coronavirus, Bovine rotavirus, Escherichia coli</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Emulsion for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Viral and Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2678418.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_451187.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2678423.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A012304</VMDProductNo>
    <Name>Porcilis Glässer Suspension for Injection for Pigs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3035</VMNo>
    <DateOfIssue>2004-03-22</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Haemophilus parasuis </ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_182869.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2922381.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A012179</VMDProductNo>
    <Name>Nobivac DHP</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3036</VMNo>
    <DateOfIssue>2005-07-28</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Canine adenovirus, Canine distemper virus, Canine parvovirus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate and solvent for suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_168930.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_1989939.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2741692.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A011378</VMDProductNo>
    <Name>AquaVac Relera Concentrate for Dip Suspension or Suspension for Injection for Rainbow Trout</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Yersinia ruckeri</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Trout - Golden/Rainbow/Redband/Steelhead</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_244408.PDF</SPC_Link>
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    <VMDProductNo>A014123</VMDProductNo>
    <Name>Cocci-Drench 2.5 mg/ml Oral Suspension</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd.&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3038</VMNo>
    <DateOfIssue>2019-11-21</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Diclazuril</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Sheep</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
    <TherapeuticGroup>Antiprotozoal anticoccidial</TherapeuticGroup>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A014124</VMDProductNo>
    <Name>Molecoxan 2.5 mg/ml Oral Suspension</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Mole Valley Farmers Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3039</VMNo>
    <DateOfIssue>2020-07-29</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Diclazuril</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Sheep</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
    <TherapeuticGroup>Antiprotozoal anticoccidial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_1889704.PDF</SPC_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012407</VMDProductNo>
    <Name>Regumate Equine 2.2 mg/ml Oral Solution for Horses</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3040</VMNo>
    <DateOfIssue>2005-04-05</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Altrenogest</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Horses</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Oral solution</PharmaceuticalForm>
    <TherapeuticGroup>Hormone sex</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2968057.PDF</SPC_Link>
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    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2968099.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A014125</VMDProductNo>
    <Name>Vecoxan 2.5 mg/ml Oral Suspension</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3041</VMNo>
    <DateOfIssue>1999-02-03</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Diclazuril</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Sheep</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
    <TherapeuticGroup>Antiprotozoal anticoccidial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_141342.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2968212.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012660</VMDProductNo>
    <Name>Vidalta 10 mg Prolonged-release Tablets for Cats</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3042</VMNo>
    <DateOfIssue>2007-12-21</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Carbimazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Prolonged-release tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anti Hormone Agent</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2771318.PDF</SPC_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012661</VMDProductNo>
    <Name>Vidalta 15 mg Prolonged-release Tablets for Cats</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3043</VMNo>
    <DateOfIssue>2007-12-21</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Carbimazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Prolonged-release tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anti Hormone Agent</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2771352.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_361701.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2771359.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A014126</VMDProductNo>
    <Name>Paracox-8, Suspension for Oral Suspension for Chickens</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3044</VMNo>
    <DateOfIssue>1998-08-10</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Eimeria acervulina, Eimeria brunetti, Eimeria maxima, Eimeria mitis, Eimeria necatrix, Eimeria praecox, Eimeria tenella</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Suspension for oral suspension</PharmaceuticalForm>
    <TherapeuticGroup>Live Parasitic Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_138962.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2968374.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012167</VMDProductNo>
    <Name>Nobilis MG 6/85 Lyophilisate for Suspension for Chickens</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3045</VMNo>
    <DateOfIssue>2002-02-21</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Mycoplasma gallisepticum</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate for suspension</PharmaceuticalForm>
    <TherapeuticGroup>Live Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2616582.PDF</SPC_Link>
    <UKPAR_Link />
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012686</VMDProductNo>
    <Name>Zitac Vet 100 mg Tablets for Dogs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3046</VMNo>
    <DateOfIssue>2007-02-22</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Cimetidine</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Gastrointestinal anti-emetic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2993617.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2993641.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012687</VMDProductNo>
    <Name>Zitac Vet 200 mg Tablets for Dogs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3047</VMNo>
    <DateOfIssue>2007-02-22</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Cimetidine</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Gastrointestinal anti-emetic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2993569.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2993584.PDF</PAAR_Link>
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    <VMDProductNo>A012210</VMDProductNo>
    <Name>Nuflor Minidose 450 mg/ml Solution for Injection for Cattle</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3048</VMNo>
    <DateOfIssue>2008-10-03</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Florfenicol</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2607122.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_1964917.PDF</UKPAR_Link>
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    <VMDProductNo>A014183</VMDProductNo>
    <Name>Nobilis ND Clone 30 Live Lyophilisate for Oculonasal Suspension/Use in Drinking Water for Chickens and Turkeys</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3049</VMNo>
    <DateOfIssue>2005-10-24</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Newcastle disease virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens, Turkeys</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate for oculonasal suspension/use in drinking water</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_184350.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3001248.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012845</VMDProductNo>
    <Name>Cepralock 2.6 g Intramammary Suspension for Dry Cows</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3050</VMNo>
    <DateOfIssue>2021-04-09</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Bismuth Subnitrate</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Intramammary suspension</PharmaceuticalForm>
    <TherapeuticGroup>Miscellaneous mechanical teat seal </TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_3000814.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3000834.PDF</PAAR_Link>
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    <VMDProductNo>A014144</VMDProductNo>
    <Name>AquaVac S7 Emulsion for Injection for Atlantic Salmon </Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors />
    <VMNo>06376/3051</VMNo>
    <DateOfIssue>2026-03-04</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Aeromonas salmonicida subsp. salmonicida, Infectious pancreatic necrosis virus, Listonella anguillarum, Moritella viscosa, Vibrio salmonicida, Yersinia ruckeri</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Atlantic salmon</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Emulsion for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Viral and Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_3207558.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link />
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012225</VMDProductNo>
    <Name>Otomax Ear Drops Suspension </Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3052</VMNo>
    <DateOfIssue>1999-07-22</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Betamethasone, Clotrimazole, Gentamicin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Ear drops, suspension</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial; Anti Inflammatory; Antimycotic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_3007792.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3007815.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012182</VMDProductNo>
    <Name>Nobivac Pi, Lyophilisate and Solvent for Suspension for Injection for Dogs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3053</VMNo>
    <DateOfIssue>2002-01-31</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Canine parainfluenza virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate and solvent for suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_107991.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3023986.PDF</PAAR_Link>
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    <VMDProductNo>A014219</VMDProductNo>
    <Name>Porcilis Ery+Parvo Suspension for Injection for Pigs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3054</VMNo>
    <DateOfIssue>1997-07-16</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Erysipelothrix rhusiopathiae, Porcine parvovirus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Viral and Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_3024253.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3024387.PDF</PAAR_Link>
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    <VMDProductNo>A012208</VMDProductNo>
    <Name>Nuflor 300 mg/ml Solution for Injection for Cattle and Sheep</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/3055</VMNo>
    <DateOfIssue>2013-02-25</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Florfenicol</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Sheep</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2965669.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_1992719.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2965699.PDF</PAAR_Link>
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    <VMDProductNo>A011377</VMDProductNo>
    <Name>AquaVac PD3 Emulsion for Injection for Atlantic Salmon</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd.&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Avian pneumovirus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate for oculonasal suspension</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd.&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <DateOfIssue>2000-08-17</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Salmonella enteritidis, Salmonella typhimurium</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Cloprostenol</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Prostaglandin</TherapeuticGroup>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Mannheimia haemolytica, Pasteurella trehalosi</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Sheep</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
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    <Name>Receptal 4 microgram/ml solution for injection </Name>
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    <Distributors>&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <Territory>Northern Ireland</Territory>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <Name>Vivitonin 50 mg Tablets for Dogs</Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Propentofylline</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Coated tablet</PharmaceuticalForm>
    <TherapeuticGroup>Cardio Vascular</TherapeuticGroup>
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    <Name>Panacur Granules 222 mg/g</Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Fenbendazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Dogs</TargetSpecies>
    <DistributionCategory>NFA-VPS</DistributionCategory>
    <PharmaceuticalForm>Granules</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <Name>Panacur 10% Oral Suspension</Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Fenbendazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <Name>Panacur Small Animal 100 mg/ml Oral Suspension</Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Fenbendazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>NFA-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <Name>Vivitonin 100 mg Tablets for Dogs</Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Propentofylline</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Cardio Vascular</TherapeuticGroup>
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    <Name>Panacur 187.5 mg/g Oral Paste for Dogs and Cats</Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Fenbendazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>NFA-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral paste</PharmaceuticalForm>
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    <Name>Imizol 85 mg/ml Solution for Injection</Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Imidocarb</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antiprotozoal</TherapeuticGroup>
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    <ActiveSubstances>Procaine Benzylpenicillin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
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    <Name>Caninsulin 40 IU/ml Suspension for Injection</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Insulin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Hormone</TherapeuticGroup>
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    <Name>Oxytocin-S, 10 iu/ml, Solution for Injection</Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <VMDProductNo>A001303</VMDProductNo>
    <Name>Dexadreson 2 mg/ml Solution for Injection</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Dexamethasone</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Anti Inflammatory corticosteroid</TherapeuticGroup>
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    <VMDProductNo>A001302</VMDProductNo>
    <Name>Dexafort Suspension for Injection</Name>
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    <AuthorisationRoute>National</AuthorisationRoute>
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    <ActiveSubstances>Fenbendazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Continuous-release intraruminal device</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Flunixin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Anti Inflammatory NSAID</TherapeuticGroup>
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    <Name>Finadyne 50 mg/ml Solution for Injection</Name>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Flunixin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <Name>Finadyne 50 mg/g Oral Paste</Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4089</VMNo>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Flunixin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Horses</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Oral paste</PharmaceuticalForm>
    <TherapeuticGroup>Anti Inflammatory NSAID</TherapeuticGroup>
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    <VMDProductNo>A000002</VMDProductNo>
    <Name>Chorulon 1500 IU Powder and Solvent for Solution for Injection</Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4090</VMNo>
    <DateOfIssue>1994-05-18</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Chorionic Gonadotrophin</ActiveSubstances>
    <ControlledDrug>4</ControlledDrug>
    <TargetSpecies>Cattle, Dogs, Horses</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Powder and solvent for solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Hormone sex</TherapeuticGroup>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Furosemide</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Cattle, Dogs, Horses</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Cardio Vascular diuretic</TherapeuticGroup>
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    <Name>Panacur Equine 222 mg/g Granules </Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited
&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Fenbendazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Horses</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Granules</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <Name>Panacur Equine Guard 100 mg/ml Oral Suspension</Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Fenbendazole</ActiveSubstances>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <Name>Panacur Equine Oral Paste 18.75% w/w</Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Fenbendazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-VPS</DistributionCategory>
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    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <Name>PG 600, Powder and Solvent for Solution for Injection</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Chorionic Gonadotrophin, Serum Gonadotrophin</ActiveSubstances>
    <ControlledDrug>4</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Powder and solvent for solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Hormone sex</TherapeuticGroup>
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    <Name>PMSG Intervet 5000IU, Powder and Solvent for Solution for Injection</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Serum Gonadotrophin</ActiveSubstances>
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    <PharmaceuticalForm>Powder and solvent for solution for injection</PharmaceuticalForm>
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    <Name>Regumate Porcine, 0.4% w/v Oral Solution</Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <DateOfIssue>1985-11-12</DateOfIssue>
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    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Altrenogest</ActiveSubstances>
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    <DistributionCategory>POM-V</DistributionCategory>
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    <Name>Metricure 500 mg Intrauterine Suspension</Name>
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    <Name>Deltamole 7.5 mg/ml Pour-on Suspension for Cattle</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Mole Valley Farmers Ltd&lt;/span&gt;</Distributors>
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    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Deltamethrin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-VPS</DistributionCategory>
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    <VMDProductNo>A000451</VMDProductNo>
    <Name>Toxovax Concentrate and Solvent for Suspension for Injection for Sheep</Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <Territory>United Kingdom</Territory>
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    <PharmaceuticalForm>Concentrate for solution for injection</PharmaceuticalForm>
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    <Name>Enzovax </Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <PharmaceuticalForm>Powder for suspension for injection</PharmaceuticalForm>
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    <Name>Nobivac Rabies suspension for injection</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4106</VMNo>
    <DateOfIssue>2005-10-25</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Rabies virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_184364.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_561293.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A003500</VMDProductNo>
    <Name>Canigen DHPPi Lyophilisate for Suspension for Injection for Dogs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
    <VMNo>06376/4107</VMNo>
    <DateOfIssue>2005-10-20</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Canine adenovirus, Canine distemper virus, Canine parainfluenza virus, Canine parvovirus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Powder for suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_144299.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_531000.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A007027</VMDProductNo>
    <Name>Canigen Parvo-C Lyophilisate for Suspension for Injection</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
    <VMNo>06376/4108</VMNo>
    <DateOfIssue>2007-08-01</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Canine parvovirus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_188387.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_360857.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_405982.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A006054</VMDProductNo>
    <Name>Canigen Rabies</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
    <VMNo>06376/4109</VMNo>
    <DateOfIssue>2005-10-25</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Rabies virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_139712.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_536236.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A002927</VMDProductNo>
    <Name>Footvax Emulsion for Injection for Sheep</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited
&lt;/span&gt;</Distributors>
    <VMNo>06376/4110</VMNo>
    <DateOfIssue>2005-10-28</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Dichelobacter nodosus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Sheep</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Emulsion for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_142559.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_546704.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A001320</VMDProductNo>
    <Name>Lambivac</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited
&lt;/span&gt;</Distributors>
    <VMNo>06376/4111</VMNo>
    <DateOfIssue>2005-10-17</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Clostridium perfringens, Clostridium tetani</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs, Sheep</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_139709.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_553407.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A002921</VMDProductNo>
    <Name>Bovilis Leptavoid–H Suspension for Injection for Cattle</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4112</VMNo>
    <DateOfIssue>2005-10-24</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Leptospira hardjo</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_141252.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_554314.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A006702</VMDProductNo>
    <Name>Canigen DHP</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
    <VMNo>06376/4114</VMNo>
    <DateOfIssue>2006-04-21</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Canine adenovirus, Canine distemper virus, Canine parvovirus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate for suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_153427.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_360855.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_260670.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A006057</VMDProductNo>
    <Name>Canigen KC</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
    <VMNo>06376/4115</VMNo>
    <DateOfIssue>2003-08-29</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Bordetella bronchiseptica, Canine parainfluenza virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Nasal spray, lyophilisate and solvent for suspension</PharmaceuticalForm>
    <TherapeuticGroup>Live Bacterial and Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_124265.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_536142.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A006056</VMDProductNo>
    <Name>Canigen Pi Lyophilisate and Solvent for Suspension for Injection for Dogs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Virbac Ltd&lt;/span&gt;</Distributors>
    <VMNo>06376/4116</VMNo>
    <DateOfIssue>2003-08-26</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Canine parainfluenza virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_124273.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_536204.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A002554</VMDProductNo>
    <Name>Nobilis Ma5 + Clone 30 Lyophilisate for Oculonasal Suspension/use in Drinking Water for Chickens</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4117</VMNo>
    <DateOfIssue>1997-02-20</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Infectious bronchitis virus, Newcastle disease virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate for oculonasal suspension/use in drinking water</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_184244.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_557555.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A002472</VMDProductNo>
    <Name>Ovivac P Plus Suspension for Injection for Sheep</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4119</VMNo>
    <DateOfIssue>1996-11-27</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Clostridium chauvoei, Clostridium perfringens, Clostridium septicum, Clostridium tetani, Mannheimia haemolytica, Pasteurella trehalosi</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Sheep</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_214961.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_559157.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A002636</VMDProductNo>
    <Name>Nobilis Gumboro 228E Lyophilisate for Use in Drinking Water for Chickens </Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4120</VMNo>
    <DateOfIssue>1997-04-04</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Infectious bursal disease virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Powder for oral suspension</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_124314.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_551550.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A000506</VMDProductNo>
    <Name>Nobilis Gumboro D78 Lyophilisate for Oculonasal Suspension/Use in Drinking Water for Chickens</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4121</VMNo>
    <DateOfIssue>1994-02-15</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Infectious bursal disease virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_124286.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_551777.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A002532</VMDProductNo>
    <Name>Receptal 4 microgram/ml Solution for Injection </Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4122</VMNo>
    <DateOfIssue>1993-05-28</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Buserelin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Horses, Pigs, Rabbits, Trout</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Hormone</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_92720.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_330916.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_571489.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A007421</VMDProductNo>
    <Name>Nobilis Erysipelas Suspension for Injection for Turkeys</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited
&lt;/span&gt;</Distributors>
    <VMNo>06376/4123</VMNo>
    <DateOfIssue>2009-06-26</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Erysipelothrix rhusiopathiae</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Turkeys</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_253894.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_263817.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_261284.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A001451</VMDProductNo>
    <Name>Nobilis Rismavac Concentrate and Solvent for Suspension for Injection for Chickens</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4124</VMNo>
    <DateOfIssue>1994-02-24</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Marek's disease virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_136704.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_558936.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A002976</VMDProductNo>
    <Name>Nobilis Rismavac + CA126 Concentrate and Solvent for Suspension for Injection for Chickens </Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4125</VMNo>
    <DateOfIssue>1997-11-13</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Marek's disease virus, Turkey herpesvirus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_124298.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_559011.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A001661</VMDProductNo>
    <Name>Nobivac Solvent</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4126</VMNo>
    <DateOfIssue>2005-10-28</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>See SPC</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Diluent</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_143842.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_631354.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A002893</VMDProductNo>
    <Name>Ceporex 180 mg/ml Suspension for Injection for Cattle, Cats and Dogs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4127</VMNo>
    <DateOfIssue>1992-12-23</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Cefalexin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Cattle, Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_138704.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_536587.PDF</PAAR_Link>
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    <VMDProductNo>A002913</VMDProductNo>
    <Name>Cepravin Dry Cow 250 mg Intramammary Suspension</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <DateOfIssue>1993-01-01</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Cephalonium</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Intramammary suspension</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial intramammary</TherapeuticGroup>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A002674</VMDProductNo>
    <Name>Cobactan MC Intramammary Ointment 75 mg for Lactating Cows</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4129</VMNo>
    <DateOfIssue>1997-05-29</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Cefquinome</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Intramammary suspension</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial intramammary</TherapeuticGroup>
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    <Name>Florocol Premix for Medicated Feeding Stuff 500mg/g for Atlantic Salmon</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4130</VMNo>
    <DateOfIssue>1999-09-13</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Florfenicol</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Atlantic salmon</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Premix for medicated feeding stuff</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
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    <VMDProductNo>A006502</VMDProductNo>
    <Name>Nobilis Diluent Oculo Nasal</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4131</VMNo>
    <DateOfIssue>2005-11-09</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>See SPC</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Poultry</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Diluent</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_142776.PDF</SPC_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A001254</VMDProductNo>
    <Name>Nobilis IB + ND + EDS Emulsion for Injection for Chickens</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4132</VMNo>
    <DateOfIssue>2005-10-19</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Avian infectious bronchitis virus, Egg drop syndrome virus, Newcastle disease virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Emulsion for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_139715.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_551788.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A001927</VMDProductNo>
    <Name>Nobilis REO Inac Emulsion for Injection for Chickens</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4133</VMNo>
    <DateOfIssue>1995-06-24</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Avian reovirus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Emulsion for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_124296.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_558741.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A001216</VMDProductNo>
    <Name>Optimmune 2 mg/g Eye Ointment for Dogs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4134</VMNo>
    <DateOfIssue>1994-06-09</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Ciclosporin A</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Eye ointment</PharmaceuticalForm>
    <TherapeuticGroup>Anti Inflammatory immunosuppressive</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_138967.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_551368.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A003218</VMDProductNo>
    <Name>Engemycin 10% Farm Pack Solution for Injection</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4135</VMNo>
    <DateOfIssue>1998-08-27</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Oxytetracycline</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Horses, Pigs, Sheep</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_138033.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_544518.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A002223</VMDProductNo>
    <Name>Engemycin 10% DD Solution for Injection</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4136</VMNo>
    <DateOfIssue>1995-12-11</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Oxytetracycline</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Cattle, Dogs, Horses, Pigs, Sheep</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_138456.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_544416.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A001148</VMDProductNo>
    <Name>Bovilis Huskvac Oral Suspension for Cattle</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4137</VMNo>
    <DateOfIssue>2005-09-23</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Dictyocaulus viviparus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
    <TherapeuticGroup>Live Parasitic Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_138875.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_534239.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A002723</VMDProductNo>
    <Name>Porcilis Ery Suspension for Injection for Pigs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited
&lt;/span&gt;</Distributors>
    <VMNo>06376/4138</VMNo>
    <DateOfIssue>1997-07-07</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Erysipelothrix rhusiopathiae</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_141244.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_552207.PDF</PAAR_Link>
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    <VMDProductNo>A000090</VMDProductNo>
    <Name>Nobilis IB Ma5 Lyophilisate for Oculonasal Suspension / Use in Drinking Water for Chickens</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4139</VMNo>
    <DateOfIssue>2005-10-25</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Infectious bronchitis virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate for suspension</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_144044.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_551797.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A001689</VMDProductNo>
    <Name>Tetanus Antitoxin Behring Solution for Injection for Horses, Sheep and Dogs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/4140</VMNo>
    <DateOfIssue>2005-10-14</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>United Kingdom</Territory>
    <ActiveSubstances>Clostridium tetani, Equine plasma</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs, Horses, Sheep</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antisera</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_139981.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_578608.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A005649</VMDProductNo>
    <Name>Scalibor Protectorband 0.76 g Medicated Collar for Small and Medium Sized Dogs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/5000</VMNo>
    <DateOfIssue>2002-03-21</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Deltamethrin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>NFA-VPS</DistributionCategory>
    <PharmaceuticalForm>Collar</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_114758.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_567542.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A005650</VMDProductNo>
    <Name>Scalibor Protectorband 1.0 g Medicated Collar for Large Sized Dogs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/5001</VMNo>
    <DateOfIssue>2002-03-21</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Deltamethrin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>NFA-VPS</DistributionCategory>
    <PharmaceuticalForm>Collar</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_114757.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_555627.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A006851</VMDProductNo>
    <Name>Resflor 300/16.5 mg/ml Solution for Injection for Cattle</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/5002</VMNo>
    <DateOfIssue>2006-10-19</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Florfenicol, Flunixin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial; Anti Inflammatory</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_165169.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_260743.PDF</PAAR_Link>
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    <VMDProductNo>A006485</VMDProductNo>
    <Name>Chronogest CR, 20 mg Controlled Release Vaginal Sponge for Sheep</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/5003</VMNo>
    <DateOfIssue>2005-06-21</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Flugestone Acetate</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Sheep</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Vaginal sponge</PharmaceuticalForm>
    <TherapeuticGroup>Hormone sex</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_122282.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_537438.PDF</PAAR_Link>
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    <VMDProductNo>A006947</VMDProductNo>
    <Name>Mastiplan LC, 300 mg/20 mg (Cefapirin/Prednisolone), Intramammary Suspension for Lactating Cows </Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/5004</VMNo>
    <DateOfIssue>2007-05-25</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Cefapirin, Prednisolone</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Intramammary suspension</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial intramammary; Anti Inflammatory</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_176372.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_436657.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A003868</VMDProductNo>
    <Name>Slice 2 mg/g Premix for Medicated Feeding Stuff</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>06376/5005</VMNo>
    <DateOfIssue>2000-01-13</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Emamectin Benzoate</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Atlantic salmon</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Premix for medicated feeding stuff</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_154091.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_1463026.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_573752.PDF</PAAR_Link>
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    <VMDProductNo>A010561</VMDProductNo>
    <Name>Porcilis Lawsonia ID Lyophilisate and Solvent for Emulsion for Injection for Pigs</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Ltd&lt;/span&gt;</Distributors>
    <VMNo>06376/5006</VMNo>
    <DateOfIssue>2020-12-23</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Lawsonia intracellularis</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate and solvent for emulsion for injection</PharmaceuticalForm>
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    <Name>Nobilis RT + IBmulti + G + ND</Name>
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    <Name>Nobivac Ducat</Name>
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    <Name>Nobilis Salenvac ETC Suspension for Injection for Chickens</Name>
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    <Name>Bovilis Bovivac S</Name>
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    <Name>Heptavac P Plus Suspension for Injection for Sheep</Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
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    <Name>Bovilis IBR Marker Live, Lyophilisate and Solvent for Suspension for Cattle</Name>
    <MAHolder>Intervet International B.V.</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Infectious bovine rhinotraceitis virus</ActiveSubstances>
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    <Name>Nobivac Respira Bb Suspension for Injection for Dogs </Name>
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    <Distributors>&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
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    <Distributors>&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <DistributionCategory>POM-VPS</DistributionCategory>
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    <Distributors>&lt;span&gt;Intervet Ireland Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <Name>Nobilis Salenvac T Suspension for Injection for Chickens</Name>
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    <Distributors>&lt;span&gt;Intervet Ireland Ltd.&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
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    <Name>Clavaseptin 250 mg Palatable Tablets for Dogs</Name>
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    <DistributionCategory>POM-V</DistributionCategory>
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&lt;/span&gt;</Distributors>
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    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
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    <ActiveSubstances>Febantel, Praziquantel, Pyrantel Embonate</ActiveSubstances>
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    <DistributionCategory>NFA-VPS</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
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    <DistributionCategory>NFA-VPS</DistributionCategory>
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    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
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    <Name>Albex 10% w/v Oral Suspension</Name>
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    <Territory>Northern Ireland</Territory>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
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    <ActiveSubstances>Albendazole</ActiveSubstances>
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    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <Name>Chanaverm 7.5% Oral Solution</Name>
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    <Name>Clinacin 300 mg Tablets for Dogs</Name>
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    <DateOfIssue>2010-02-10</DateOfIssue>
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    <ActiveSubstances>Clindamycin</ActiveSubstances>
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    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
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    <Name>Zerofen Worm Drench 10% w/v Oral Suspension for Sheep and Cattle</Name>
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    <ActiveSubstances>Fenbendazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <Name>Johnson’s Guardian Plus Spot-On Solution for Cats </Name>
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    <Distributors>&lt;span&gt;Johnson’s Veterinary Products Ltd&lt;/span&gt;</Distributors>
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    <DateOfIssue>2021-11-15</DateOfIssue>
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    <ActiveSubstances>(S)-Methoprene, Fipronil</ActiveSubstances>
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    <DistributionCategory>AVM-GSL</DistributionCategory>
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    <Name>Premadex 0.5% w/v Pour-on Solution</Name>
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    <Distributors>&lt;span&gt;Downland Marketing Ltd&lt;/span&gt;</Distributors>
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    <Name>ITCH FLEA 268 mg/241.2 mg Spot-on Solution for Large Dogs</Name>
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    <Name>ITCH FLEA 402 mg/361.8 mg Spot-on Solution for Extra Large Dogs</Name>
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    <Name>ITCH FLEA 50 mg/60 mg Spot-on Solution for Cats</Name>
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    <Name>ITCH FLEA 67 mg/60.3 mg Spot-on Solution for Small Dogs</Name>
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    <DateOfIssue>2018-08-08</DateOfIssue>
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    <VMDProductNo>A013277</VMDProductNo>
    <Name>Ridamec LA 100 mg/ml Solution for Injection for Cattle  </Name>
    <MAHolder>Chanelle Pharmaceuticals Manufacturing Ltd</MAHolder>
    <Distributors />
    <VMNo>08749/3068</VMNo>
    <DateOfIssue>2024-09-09</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Moxidectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Endectocide</TherapeuticGroup>
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    <Name>Albacert 2.5% w/v SC Oral Suspension</Name>
    <MAHolder>Chanelle Pharmaceuticals Manufacturing Ltd</MAHolder>
    <Distributors>&lt;span&gt;Downland Marketing Limited&lt;/span&gt;</Distributors>
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    <Territory>Northern Ireland</Territory>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
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    <Name>Beaphar One Dose Small Dog Wormer 100 mg Nitroscanate Film-coated Tablets</Name>
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    <Distributors>&lt;span&gt;Johnson's Veterinary Products Ltd&lt;/span&gt;</Distributors>
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    <Distributors>&lt;span&gt;Johnson's Veterinary Products Ltd&lt;/span&gt;</Distributors>
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    <MAHolder>Chanelle Pharmaceuticals Manufacturing Ltd</MAHolder>
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    <DistributionCategory>AVM-GSL</DistributionCategory>
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    <Distributors>&lt;span&gt;Chanelle Animal Health Ltd&lt;/span&gt;</Distributors>
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    <DateOfIssue>2018-08-08</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>(S)-Methoprene, Fipronil</ActiveSubstances>
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    <DistributionCategory>AVM-GSL</DistributionCategory>
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    <MAHolder>Chanelle Pharmaceuticals Manufacturing Ltd</MAHolder>
    <Distributors>&lt;span&gt;Chanelle Animal Health Ltd&lt;/span&gt;</Distributors>
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    <DateOfIssue>2018-08-08</DateOfIssue>
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    <MAHolder>Chanelle Pharmaceuticals Manufacturing Ltd</MAHolder>
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    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
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    <Name>Wormit Plus 12.5 mg/125 mg Flavoured Tablets for Dogs (Milbemycin / Praziquantel) </Name>
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    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <MAHolder>Chanelle Pharmaceuticals Manufacturing Ltd</MAHolder>
    <Distributors />
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    <DateOfIssue>2020-01-29</DateOfIssue>
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    <Territory>Northern Ireland</Territory>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
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    <DateOfIssue>2020-01-29</DateOfIssue>
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    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
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    <Distributors>&lt;span&gt;Chanelle Vet UK Ltd
&lt;/span&gt;</Distributors>
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    <ControlledDrug>N</ControlledDrug>
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    <Distributors>&lt;span&gt;Chanelle Vet UK Ltd
&lt;/span&gt;</Distributors>
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&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National</AuthorisationRoute>
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    <Territory>Great Britain</Territory>
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    <ControlledDrug>N</ControlledDrug>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Oral solution</PharmaceuticalForm>
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    <Distributors>&lt;span&gt;Vetoquinol UK Limited&lt;/span&gt;</Distributors>
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    <Territory>Great Britain</Territory>
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    <DistributionCategory>AVM-GSL</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
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    <DistributionCategory>AVM-GSL</DistributionCategory>
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    <DistributionCategory>AVM-GSL</DistributionCategory>
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    <Name>Moxidectin EU Pharmaceuticals 5 mg/ml Pour-on Solution for Cattle </Name>
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    <Distributors />
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Moxidectin</ActiveSubstances>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
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    <Name>Ezi-Wormer Duo 12.5 mg/125 mg Flavoured Tablets for Dogs (Milbemycin / Praziquantel)</Name>
    <MAHolder>Chanelle Pharmaceuticals Manufacturing Ltd</MAHolder>
    <Distributors />
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    <DateOfIssue>2020-01-29</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
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&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Turkey herpesvirus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DateOfIssue>2020-09-21</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <ActiveSubstances>Clindamycin</ActiveSubstances>
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    <ActiveSubstances>Actinobacillus pleuropneumoniae</ActiveSubstances>
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    <Name>Kesium 50 mg / 12.5 mg Chewable Tablets for Cats and Dogs</Name>
    <MAHolder>Ceva Sante Animale</MAHolder>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
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&lt;/span&gt;</Distributors>
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    <Distributors>&lt;span&gt;Nutrapet Ltd&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Iron</ActiveSubstances>
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    <Name>Apitraz 500 mg Bee-hive Strips for Honey Bees</Name>
    <MAHolder>Laboratorios Calier, S.A.</MAHolder>
    <Distributors>&lt;span&gt;Laboratorios Calier, SA&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Amitraz</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <PharmaceuticalForm>Bee-hive strip</PharmaceuticalForm>
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    <Name>VETERELIN 0.004 mg/ml Solution for Injection for Cattle, Horses, Pigs, and Rabbits</Name>
    <MAHolder>Laboratorios Calier, SA</MAHolder>
    <Distributors>&lt;span&gt;E.G.G. Technologies International Ltd.&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Buserelin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <Name>Veteglan 0.075 mg/ml Solution for Injection for Cows, Sows and Mares</Name>
    <MAHolder>Laboratorios Calier, SA</MAHolder>
    <Distributors>&lt;span&gt;EGG TECHNOLOGIES INTERNATIONAL LTD&lt;/span&gt;</Distributors>
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    <ActiveSubstances>d-Cloprostenol</ActiveSubstances>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <Name>Banacep Vet 5 mg Film-coated Tablet for Dogs and Cats Benazepril Hydrochloride</Name>
    <MAHolder>Laboratorios Calier, S.A.</MAHolder>
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    <ActiveSubstances>Benazepril Hydrochloride</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
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    <Distributors>&lt;span&gt;Laboratorios Calier S.A.&lt;/span&gt;</Distributors>
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    <Distributors>&lt;span&gt;Laboratorios Calier S.A.&lt;/span&gt;</Distributors>
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    <Distributors>&lt;span&gt;EGG TECHNOLOGIES INTERNATIONAL LTD&lt;/span&gt;</Distributors>
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    <Name>Zipyran 50 mg/50 mg/150 mg tablets for dogs</Name>
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    <Distributors>&lt;span&gt;Laboratorios Calier S.A.&lt;/span&gt;</Distributors>
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    <Distributors>&lt;span&gt;Laboratorios Calier S.A.&lt;/span&gt;</Distributors>
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    <Name>Doramax 10 mg/ml Solution for Injection for Cattle and Sheep</Name>
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    <Distributors>&lt;span&gt;Animalcare Ltd&lt;/span&gt;</Distributors>
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    <Territory>Northern Ireland</Territory>
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    <Distributors>&lt;span&gt;Dechra Limited&lt;/span&gt;</Distributors>
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    <Territory>Northern Ireland</Territory>
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    <ActiveSubstances>Mycoplasma hyopneumoniae, recombinant Porcine Circovirus type 1 expressing the Porcine circovirus type 2 ORF2 protein</ActiveSubstances>
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    <Distributors>&lt;span&gt;Zoetis UK Limited&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Porcine respiratory and reproductive syndrome virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <ControlledDrug>N</ControlledDrug>
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    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
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    <ControlledDrug>N</ControlledDrug>
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    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate and suspension for suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral and Inactivated Viral and Bacterial Vaccine</TherapeuticGroup>
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    <ActiveSubstances>Canine adenovirus, Canine distemper virus, Canine parainfluenza virus, Canine parvovirus</ActiveSubstances>
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    <Distributors>&lt;span&gt;Zoetis UK Limited&lt;/span&gt;</Distributors>
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    <Distributors>&lt;span&gt;Bimeda Animal Health Limited&lt;/span&gt;</Distributors>
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    <Name>Cronyxin 50 mg/g Oral Paste for Horses </Name>
    <MAHolder>Bimeda Animal Health Limited</MAHolder>
    <Distributors>&lt;span&gt;DUGV (UK) Ltd.&lt;/span&gt;</Distributors>
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    <Distributors>&lt;span&gt;Cross Vetpharm Group UK Ltd (Trading as Bimeda)&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Diclazuril</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
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    <Name>Gamrozyne 150 mg/ml Solution for Injection for Cattle, Sheep and Pigs</Name>
    <MAHolder>Bimeda Animal Health Limited</MAHolder>
    <Distributors>&lt;span&gt;Bimeda Animal Health Limited&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Gamithromycin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Pigs, Sheep</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
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    <Name>Vectin Horse Oral Paste, 18.7 mg/g</Name>
    <MAHolder>Bimeda Animal Health Limited</MAHolder>
    <Distributors>&lt;span&gt;Intervet Ireland Ltd&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;MSD Animal Health UK Limited&lt;/span&gt;</Distributors>
    <VMNo>50146/3006</VMNo>
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    <Territory>Northern Ireland</Territory>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral paste</PharmaceuticalForm>
    <TherapeuticGroup>Endectocide</TherapeuticGroup>
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    <Name>Maximec Horse Oral Paste, 18.7 mg/g</Name>
    <MAHolder>Bimeda Animal Health Limited</MAHolder>
    <Distributors>&lt;span&gt;Eli Lilly and Company Limited&lt;/span&gt;</Distributors>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Ivermectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <PharmaceuticalForm>Oral paste</PharmaceuticalForm>
    <TherapeuticGroup>Endectocide</TherapeuticGroup>
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    <Name>Cosecure Cattle Bolus Continuous Release Intraruminal Device</Name>
    <MAHolder>Bimeda Animal Health Limited</MAHolder>
    <Distributors>&lt;span&gt;Bimeda (Division of Cross Vetpharm Group (UK) Ltd)&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Cobalt, Copper, Selenium</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Continuous-release intraruminal device</PharmaceuticalForm>
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    <Name>Bimectin 10 mg/ml Solution for Injection for Cattle, Sheep and Pigs</Name>
    <MAHolder>Bimeda Animal Health Limited</MAHolder>
    <Distributors>&lt;span&gt;Bimeda ®&lt;/span&gt;</Distributors>
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    <PharmaceuticalForm>Capsule, hard</PharmaceuticalForm>
    <TherapeuticGroup>Anti Hormone Agent</TherapeuticGroup>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012651</VMDProductNo>
    <Name>Vetoryl 30 mg Hard Capsules for Dogs</Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors>&lt;span&gt;Dechra Veterinary Products Limited&lt;/span&gt;</Distributors>
    <VMNo>50406/3016</VMNo>
    <DateOfIssue>2005-04-13</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Trilostane</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Capsule, hard</PharmaceuticalForm>
    <TherapeuticGroup>Anti hormone Agent</TherapeuticGroup>
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  <CurrentAuthorisedProducts>
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    <Name>Vetoryl 5 mg Hard Capsules for Dogs</Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors />
    <VMNo>50406/3017</VMNo>
    <DateOfIssue>2021-02-19</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Trilostane</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Capsule, hard</PharmaceuticalForm>
    <TherapeuticGroup>Anti Hormone Agent</TherapeuticGroup>
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    <UKPAR_Link />
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012652</VMDProductNo>
    <Name>Vetoryl 60 mg Hard Capsules for Dogs</Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors>&lt;span&gt;Dechra Veterinary Products Limited&lt;/span&gt;</Distributors>
    <VMNo>50406/3018</VMNo>
    <DateOfIssue>2005-04-04</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Trilostane</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Capsule, hard</PharmaceuticalForm>
    <TherapeuticGroup>Anti Hormone Agent</TherapeuticGroup>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A011791</VMDProductNo>
    <Name>Equipalazone 1 g Oral Powder for Horses and Ponies</Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors>&lt;span&gt;Dechra Veterinary Products Limited&lt;/span&gt;</Distributors>
    <VMNo>50406/3019</VMNo>
    <DateOfIssue>2017-06-15</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Phenylbutazone</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Horses</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Oral powder</PharmaceuticalForm>
    <TherapeuticGroup>Anti Inflammatory NSAID</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2744646.PDF</SPC_Link>
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  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A012046</VMDProductNo>
    <Name>Libromide 325 mg Tablets for Dogs</Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors>&lt;span&gt;Dechra Veterinary Products Limited&lt;/span&gt;</Distributors>
    <VMNo>50406/3020	</VMNo>
    <DateOfIssue>2010-02-04</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Potassium Bromide</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Neurological Agent antiepileptic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2941534.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_349619.PDF</UKPAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A014074</VMDProductNo>
    <Name>Intra-Epicaine 20 mg/ml Solution for Injection for Horses</Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors>&lt;span&gt;Dechra Veterinary Products Limited&lt;/span&gt;</Distributors>
    <VMNo>50406/3021</VMNo>
    <DateOfIssue>1990-12-20</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Mepivacaine Hydrochloride</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Horses</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Neurological Agent local anaesthetic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2941499.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2941517.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A014075</VMDProductNo>
    <Name>Pardale-V 400 mg/9 mg Tablets </Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors>&lt;span&gt;Dechra Veterinary Products Limited&lt;/span&gt;</Distributors>
    <VMNo>50406/3022	</VMNo>
    <DateOfIssue>1993-04-15</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Codeine Phosphate, Paracetamol</ActiveSubstances>
    <ControlledDrug>5</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Neurological Agent analgesic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_134468.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2941662.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A014076</VMDProductNo>
    <Name>Somulose 400 mg/ml + 25 mg/ml Solution for Injection</Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors>&lt;span&gt;Dechra Veterinary Products Limited&lt;/span&gt;</Distributors>
    <VMNo>50406/3023</VMNo>
    <DateOfIssue>2004-03-08</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Cinchocaine Hydrochloride, Secobarbital Sodium</ActiveSubstances>
    <ControlledDrug>2</ControlledDrug>
    <TargetSpecies>Cats, Cattle, Dogs, Horses</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Neurological Agent euthanasia agent</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_110326.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2941732.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A014138</VMDProductNo>
    <Name>Prednidale 25 mg Tablets for Dogs</Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors>&lt;span&gt;Dechra Veterinary Products Limited&lt;/span&gt;</Distributors>
    <VMNo>50406/3024</VMNo>
    <DateOfIssue>2007-11-19</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Prednisolone</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anti Inflammatory corticosteroid</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2974718.PDF</SPC_Link>
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  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A014140</VMDProductNo>
    <Name>Sterilised Water for Injections BP</Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors>&lt;span&gt;Dechra Veterinary Products Limited&lt;/span&gt;</Distributors>
    <VMNo>50406/3026</VMNo>
    <DateOfIssue>1994-10-25</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Water For Injections</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>All species</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solvent for parenteral use</PharmaceuticalForm>
    <TherapeuticGroup>Diluent</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2975508.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2975516.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A012004</VMDProductNo>
    <Name>Intubeaze 20 mg/ml Laryngopharyngeal Spray, Solution for Cats </Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors />
    <VMNo>50406/3027</VMNo>
    <DateOfIssue>2018-11-01</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Lidocaine Hydrochloride</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Laryngopharyngeal Spray, Solution</PharmaceuticalForm>
    <TherapeuticGroup>Neurological Agent local anaesthetic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2975501.PDF</SPC_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A014141</VMDProductNo>
    <Name>Tri-Solfen Cutaneous Solution for Pigs</Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors>&lt;span&gt;Dechra Veterinary Products&lt;/span&gt;</Distributors>
    <VMNo>50406/3028</VMNo>
    <DateOfIssue>2022-01-25</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Bupivacaine, Cetrimide, Epinephrine, Lidocaine</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Cutaneous solution</PharmaceuticalForm>
    <TherapeuticGroup>Neurological Agent local anaesthetic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2975520.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_1959232.PDF</UKPAR_Link>
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  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A011609</VMDProductNo>
    <Name>Cosacthen 0.25 mg/ml Solution for Injection for Dogs</Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors>&lt;span&gt;Dechra Veterinary Products&lt;/span&gt;</Distributors>
    <VMNo>50406/3029</VMNo>
    <DateOfIssue>2019-12-16</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Tetracosactide</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Hormone</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2995736.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_1987321.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2995759.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A014173</VMDProductNo>
    <Name>Equipalazone 1 g Oral Paste </Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors>&lt;span&gt;Dechra Veterinary Products Limited&lt;/span&gt;</Distributors>
    <VMNo>50406/3030</VMNo>
    <DateOfIssue>1994-08-26</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Phenylbutazone</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Horses</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Oral paste</PharmaceuticalForm>
    <TherapeuticGroup>Anti Inflammatory NSAID</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2996604.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2996646.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A013337</VMDProductNo>
    <Name>Felimazole 5 mg/ml Oral Solution for Cats</Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors />
    <VMNo>50406/3031</VMNo>
    <DateOfIssue>2023-10-03</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Thiamazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Oral solution</PharmaceuticalForm>
    <TherapeuticGroup>Anti Hormone Agent</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2643761.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2872333.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A011989</VMDProductNo>
    <Name>HY-50 Vet 17 mg/ml Solution for Injection</Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors>&lt;span&gt;Dechra Veterinary Products Limited&lt;/span&gt;</Distributors>
    <VMNo>50406/3032</VMNo>
    <DateOfIssue>1998-06-12</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Sodium Hyaluronate</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Horses</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Anti Inflammatory</TherapeuticGroup>
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    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2996885.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A011995</VMDProductNo>
    <Name>Hypertonic 72 mg/ml Solution for Infusion for Cattle, Cattle (Calves), Horses, Dogs and Cats</Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors>&lt;span&gt;Dechra Veterinary Products Limited&lt;/span&gt;</Distributors>
    <VMNo>50406/3033</VMNo>
    <DateOfIssue>2017-11-16</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Sodium Chloride</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Cattle, Dogs, Horses</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for infusion</PharmaceuticalForm>
    <TherapeuticGroup>Replacement Agent</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_1283671.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_1285653.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2928393.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A014174</VMDProductNo>
    <Name>Vetivex 18 (Sodium Chloride 0.18% w/v and Glucose 4% w/v Intravenous Infusion B.P. (Vet))</Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors>&lt;span&gt;Dechra Veterinary Products Limited&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;Warner Chilcott UK Limited&lt;/span&gt;</Distributors>
    <VMNo>50406/3034</VMNo>
    <DateOfIssue>1998-12-09</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Glucose, Sodium Chloride</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Cattle, Dogs, Horses</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for infusion</PharmaceuticalForm>
    <TherapeuticGroup>Replacement Agent</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2997012.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2997047.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012550</VMDProductNo>
    <Name>Tialin 125 mg/ml Solution for Use in Drinking Water for Pigs, Chickens and Turkeys</Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors>&lt;span&gt;Dechra Veterinary Products Limited&lt;/span&gt;</Distributors>
    <VMNo>50406/3036</VMNo>
    <DateOfIssue>2018-07-20</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Tiamulin Hydrogen Fumarate</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens, Pigs, Turkeys</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for use in drinking water</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2462827.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_1470218.PDF</UKPAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A014196</VMDProductNo>
    <Name>Equipalazone 200 mg/ml Solution for Injection</Name>
    <MAHolder>Dechra Regulatory B.V.</MAHolder>
    <Distributors>&lt;span&gt;Dechra Veterinary Products Limited&lt;/span&gt;</Distributors>
    <VMNo>50406/3037</VMNo>
    <DateOfIssue>1994-08-26</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Phenylbutazone</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Horses</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Anti Inflammatory NSAID</TherapeuticGroup>
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    <Distributors>&lt;span&gt;Alpha-Vet Allatgyogyaszati Kft.&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Flubendazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <Name>DrySeal 2.6 g Intramammary Suspension for Cattle</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco GmbH&lt;/span&gt;</Distributors>
    <VMNo>52127/3000</VMNo>
    <DateOfIssue>2024-08-09</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Bismuth Subnitrate</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Intramammary suspension</PharmaceuticalForm>
    <TherapeuticGroup>Miscellaneous mechanical teat seal </TherapeuticGroup>
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    <VMDProductNo>A014107</VMDProductNo>
    <Name>Flukiver 50 mg/ml Oral Suspension</Name>
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    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3001</VMNo>
    <DateOfIssue>1986-12-01</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Closantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Sheep</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic flukicide</TherapeuticGroup>
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    <VMDProductNo>A014108</VMDProductNo>
    <Name>Flypor 4% w/v Pour-on Solution</Name>
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    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Permethrin (Cis:Trans 80:20)</ActiveSubstances>
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    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Pour-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <Name>Lectade Plus Powder for Oral Solution</Name>
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    <Distributors>&lt;span&gt;Elanco AH UK Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Disodium Hydrogen Citrate, Glucose Monohydrate, Glycine, Potassium Citrate Monohydrate, Potassium Dihydrogen Phosphate, Sodium Chloride, Sodium Citrate Dihydrate </ActiveSubstances>
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    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>AVM-GSL</DistributionCategory>
    <PharmaceuticalForm>Powder for oral solution</PharmaceuticalForm>
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    <Name>AviPro Salmonella Duo Lyophilisate for Use in Drinking Water</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd.&lt;/span&gt;</Distributors>
    <VMNo>52127/3005</VMNo>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Salmonella enteritidis, Salmonella typhimurium</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens, Duck, Turkeys</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate for oculonasal suspension/use in drinking water</PharmaceuticalForm>
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    <VMDProductNo>A011408</VMDProductNo>
    <Name>Avipro Thymovac Lyophilisate for Use in Drinking Water</Name>
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    <Distributors>&lt;span&gt;Elanco Europe Ltd.&lt;/span&gt;</Distributors>
    <VMNo>52127/3006</VMNo>
    <DateOfIssue>2009-04-28</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Chicken anaemia virus strain Cux-1</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate for use in drinking water</PharmaceuticalForm>
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    <VMDProductNo>A011590</VMDProductNo>
    <Name>CLiK Extra 65 mg/ml Pour-On Suspension for Sheep</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3007</VMNo>
    <DateOfIssue>2016-10-21</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Dicyclanil</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Sheep</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Pour-on suspension</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <Name>Fortekor 2.5 mg Tablets for Cats and Dogs </Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3008</VMNo>
    <DateOfIssue>2003-03-31</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Benazepril Hydrochloride</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Cardio Vascular ACE inhibitor</TherapeuticGroup>
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    <VMDProductNo>A014127</VMDProductNo>
    <Name>ACP Injection 2 mg/ml Solution for Injection</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3009</VMNo>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Acepromazine</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Neurological Agent sedative</TherapeuticGroup>
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    <VMDProductNo>A014128</VMDProductNo>
    <Name>Corvental D 100 mg Hard Capsules</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3010</VMNo>
    <DateOfIssue>1993-02-16</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Theophylline</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Capsule, hard</PharmaceuticalForm>
    <TherapeuticGroup>Cardio Vascular; Respiratory Agent</TherapeuticGroup>
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    <Name>Corvental D 200 mg Hard Capsules</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3011</VMNo>
    <DateOfIssue>1993-02-16</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Theophylline</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <PharmaceuticalForm>Capsule, hard</PharmaceuticalForm>
    <TherapeuticGroup>Cardio Vascular; Respiratory Agent</TherapeuticGroup>
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    <Name>Corvental D 500 mg Hard Capsules</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3012</VMNo>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Theophylline</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Capsule, hard</PharmaceuticalForm>
    <TherapeuticGroup>Cardio Vascular; Respiratory Agent</TherapeuticGroup>
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    <VMDProductNo>A014131</VMDProductNo>
    <Name>Rompun 2% w/v Solution for Injection</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd.&lt;/span&gt;</Distributors>
    <VMNo>52127/3013</VMNo>
    <DateOfIssue>1995-12-14</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Xylazine</ActiveSubstances>
    <ControlledDrug>4</ControlledDrug>
    <TargetSpecies>Cats, Cattle, Dogs, Horses</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Neurological Agent sedative</TherapeuticGroup>
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    <VMDProductNo>A014163</VMDProductNo>
    <Name>Crovect 1.25% w/v Pour-on Solution for Sheep</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3014</VMNo>
    <DateOfIssue>2001-03-11</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Cypermethrin Cis 80:Trans 20</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Sheep</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Pour-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <VMDProductNo>A014164</VMDProductNo>
    <Name>Denagard 200 mg/ml Solution for Injection</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3015</VMNo>
    <DateOfIssue>1985-07-31</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Tiamulin Hydrogen Fumarate</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Pigs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
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    <VMDProductNo>A014166</VMDProductNo>
    <Name>Strongid-P Oral Paste 439 mg/g</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3016</VMNo>
    <DateOfIssue>1994-05-23</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Pyrantel Embonate</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Donkey, Horses</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral paste</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <VMDProductNo>A014167</VMDProductNo>
    <Name>Supaverm Oral Suspension</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Nitenpyram</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
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    <DistributionCategory>POM-V</DistributionCategory>
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    <TherapeuticGroup>Anti Inflammatory immunosuppressive</TherapeuticGroup>
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    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Ciclosporin A</ActiveSubstances>
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    <Name>Atopica 50 mg Soft Capsules for Dogs</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Ciclosporin A</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Capsule, soft</PharmaceuticalForm>
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    <Name>Clik 50 mg/ml Pour-on Suspension for Sheep</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco AH UK Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Pour-on suspension</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <Name>CLiKZiN 12.5 mg/ml Pour-On Suspension for Sheep</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco AH UK Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Dicyclanil</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Pour-on suspension</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <Name>Milbemax 12.5 mg/125 mg Chewable Tablets for Dogs</Name>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
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    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <Territory>Northern Ireland</Territory>
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    <Name>MilbeVet 12.5 mg/125 mg Chewable Tablets for Dogs </Name>
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    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
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    <MAHolder>Elanco GmbH</MAHolder>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
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    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Newcastle disease virus</ActiveSubstances>
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    <DistributionCategory>POM-V</DistributionCategory>
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    <Name>Fortekor Flavour 20 mg Tablets for Dogs </Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
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    <Territory>Northern Ireland</Territory>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
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    <MAHolder>Elanco GmbH</MAHolder>
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    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Triclabendazole</ActiveSubstances>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic flukicide</TherapeuticGroup>
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    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
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    <DateOfIssue>1991-08-13</DateOfIssue>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Levamisole Hydrochloride, Triclabendazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Sheep</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic flukicide</TherapeuticGroup>
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    <VMDProductNo>A014235</VMDProductNo>
    <Name>Baytril 100 mg/ml Solution for use in Drinking Water for Chickens, Turkeys and Rabbits </Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3039</VMNo>
    <DateOfIssue>1993-11-11</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Enrofloxacin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens, Rabbits, Turkeys</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for use in drinking water</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_3038798.PDF</SPC_Link>
    <UKPAR_Link />
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A014331</VMDProductNo>
    <Name>Seresto Flea and Tick Control 1.25 g + 0.56 g, Collar for Cats</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco GmbH&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3040</VMNo>
    <DateOfIssue>2017-09-04</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Flumethrin, Imidacloprid</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>NFA-VPS</DistributionCategory>
    <PharmaceuticalForm>Collar</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <UKPAR_Link />
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  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A014334</VMDProductNo>
    <Name>Seresto Flea and Tick Control 1.25 g + 0.56 g, Collar for Small Dogs ≤ 8 kg	</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd.&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3041</VMNo>
    <DateOfIssue>2017-09-04</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Flumethrin, Imidacloprid</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>NFA-VPS</DistributionCategory>
    <PharmaceuticalForm>Collar</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_1244229.PDF</SPC_Link>
    <UKPAR_Link />
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  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A014339</VMDProductNo>
    <Name>Seresto Flea and Tick Control 4.50 g + 2.03 g, Collar for Large Dogs &gt; 8 kg	</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd.&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3042</VMNo>
    <DateOfIssue>2017-09-04</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Flumethrin, Imidacloprid</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>NFA-VPS</DistributionCategory>
    <PharmaceuticalForm>Collar</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_1244300.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3073370.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A014308</VMDProductNo>
    <Name>Flubenvet 5 % w/w Premix for Medicated Feeding Stuff</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3043</VMNo>
    <DateOfIssue>2000-09-17</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Flubendazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens, Goose, Partridge, Pheasants, Turkeys</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Premix for medicated feeding stuff</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_139295.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3064448.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A014360</VMDProductNo>
    <Name>Baytril 25 mg/ml Solution for Injection</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3044</VMNo>
    <DateOfIssue>1992-04-22</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Enrofloxacin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Dogs, Ornamental Birds, Pigs, Rabbits, Reptiles, Rodents</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_3080902.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3080875.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A014361</VMDProductNo>
    <Name>Baytril 50 mg/ml Solution for Injection</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3045</VMNo>
    <DateOfIssue>1992-04-22</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Enrofloxacin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Cattle, Dogs, Goats, Pigs, Sheep</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_3081053.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3080930.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A014356</VMDProductNo>
    <Name>Baytril 100 mg/ml Solution for Injection</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3046</VMNo>
    <DateOfIssue>1993-11-11</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Enrofloxacin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Goats, Pigs, Sheep</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_3080827.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3080235.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A014342</VMDProductNo>
    <Name>Tylan Soluble Powder for Oral Solution</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3047</VMNo>
    <DateOfIssue>1993-05-25</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Tylosin Tartrate</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Chickens, Pigs, Turkeys</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Powder for oral solution</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_140142.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3074901.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A011293</VMDProductNo>
    <Name>Advantix 100 mg + 500 mg Spot-on Solution for Dogs (&gt; 4 kg ≤ 10 kg)</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3048</VMNo>
    <DateOfIssue>2003-12-23</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Imidacloprid, Permethrin (Cis:Trans 40:60)</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_110673.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3082039.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A011291</VMDProductNo>
    <Name>Advantix 250 mg + 1250 mg Spot-on Solution for Dogs (&gt; 10 kg ≤ 25 kg)</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3049</VMNo>
    <DateOfIssue>2003-12-23</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Imidacloprid, Permethrin (Cis:Trans 40:60)</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_110674.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3082198.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A011295</VMDProductNo>
    <Name>Advantix 40 mg + 200 mg Spot-on Solution for Dogs (≤ 4 kg)</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3050</VMNo>
    <DateOfIssue>2003-12-23</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Imidacloprid, Permethrin (Cis:Trans 40:60)</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_110672.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3082273.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A011292</VMDProductNo>
    <Name>Advantix 400 mg + 2000 mg Spot-on Solution for Dogs (&gt; 25 kg ≤ 40 kg)</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3051</VMNo>
    <DateOfIssue>2003-12-23</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Imidacloprid, Permethrin (Cis:Trans 40:60)</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_151145.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3082404.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A011294</VMDProductNo>
    <Name>Advantix 600 mg + 3000 mg Spot-on Solution for Dogs (&gt; 40 kg ≤ 60 kg)</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3052</VMNo>
    <DateOfIssue>2017-11-28</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Imidacloprid, Permethrin (Cis:Trans 40:60)</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_1289442.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_3086248.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A012103</VMDProductNo>
    <Name>Milbemax 4 mg/10 mg Film-coated Tablets for Small Cats and Kittens</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3053</VMNo>
    <DateOfIssue>2003-04-17</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Coated tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2499962.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2499983.PDF</PAAR_Link>
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    <VMDProductNo>A012102</VMDProductNo>
    <Name>Milbemax 16 mg/40 mg Film-coated Tablets for Cats</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3054</VMNo>
    <DateOfIssue>2003-04-17</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Coated tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2499909.PDF</SPC_Link>
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    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2499929.PDF</PAAR_Link>
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    <VMDProductNo>A012826</VMDProductNo>
    <Name>MilbeVet 16 mg/40 mg Film-coated Tablets for Cats </Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Limited&lt;/span&gt;</Distributors>
    <VMNo>52127/3055</VMNo>
    <DateOfIssue>2021-03-25</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised (Informed Consent)</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Film-coated tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2500003.PDF</SPC_Link>
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    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2500013.PDF</PAAR_Link>
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    <Name>MilbeVet 4 mg/10 mg Film-coated Tablets for Small Cats and Kittens </Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Limited&lt;/span&gt;</Distributors>
    <VMNo>52127/3056</VMNo>
    <DateOfIssue>2021-03-25</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised (Informed Consent)</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Film-coated tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2500028.PDF</SPC_Link>
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    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2500038.PDF</PAAR_Link>
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    <VMDProductNo>A012105</VMDProductNo>
    <Name>Milbemax 2.5 mg/25 mg Tablets for Small Dogs and Puppies </Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3057</VMNo>
    <DateOfIssue>2003-04-17</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2532907.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2532913.PDF</PAAR_Link>
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    <VMDProductNo>A012104</VMDProductNo>
    <Name>Milbemax 12.5 mg/125 mg Tablets for Dogs</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3058</VMNo>
    <DateOfIssue>2003-04-17</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2532886.PDF</SPC_Link>
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    <VMDProductNo>A011286</VMDProductNo>
    <Name>Advantage 40 mg Spot-on Solution for Cats (&lt;4 kg)</Name>
    <MAHolder>Elanco GmbH</MAHolder>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Ciclosporin A</ActiveSubstances>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Oral solution</PharmaceuticalForm>
    <TherapeuticGroup>Anti Inflammatory immunosuppressive</TherapeuticGroup>
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    <Name>Baytril Flavour Tablets 50 mg</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National</AuthorisationRoute>
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    <ActiveSubstances>Enrofloxacin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
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    <Name>Advantage 100 Spot-on Solution for Dogs</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3065</VMNo>
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    <AuthorisationRoute>Mutually Recognised (Informed Consent)</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Imidacloprid</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>NFA-VPS</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <Name>Advantage 250 Spot-on Solution for Dogs</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised (Informed Consent)</AuthorisationRoute>
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    <ActiveSubstances>Imidacloprid</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <Name>Advantage 40 Spot-on Solution for Dogs</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised (Informed Consent)</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Imidacloprid</ActiveSubstances>
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    <Name>Advantage 400 Spot-on Solution for Dogs</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3068</VMNo>
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    <AuthorisationRoute>Mutually Recognised (Informed Consent)</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Imidacloprid</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <VMDProductNo>A012999</VMDProductNo>
    <Name>Flyclanil 5% Pour-on Suspension for Sheep</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3069</VMNo>
    <DateOfIssue>2021-10-29</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Dicyclanil</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-VPS</DistributionCategory>
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    <VMDProductNo>A014526</VMDProductNo>
    <Name>Program 40 mg Suspension for Injection</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3070</VMNo>
    <DateOfIssue>1997-12-24</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Lufenuron</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
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    <TherapeuticGroup>Insect Growth Regulator</TherapeuticGroup>
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    <Name>Program 80 mg Suspension for Injection</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3071</VMNo>
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    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Lufenuron</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <Name>AviPro IBD Xtreme Lyophilisate for Use in Drinking Water for Chickens</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3072</VMNo>
    <DateOfIssue>2008-05-29</DateOfIssue>
    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Infectious bursal disease virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Oral lyophilisate</PharmaceuticalForm>
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    <Name>Dicyclafly 5% Pour-on Suspension for Sheep</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3073</VMNo>
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    <Territory>Northern Ireland</Territory>
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    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
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    <Name>Advantage 80 mg Spot-on Solution for Large Cats and Pet Rabbits</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
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    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
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    <Name>AviPro Precise Lyophilisate for Use in Drinking Water</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/3076</VMNo>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Infectious bursal disease virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
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    <Name>Baycox Multi 50 mg/ml Oral Suspension for Cattle, Pigs and Sheep</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Toltrazuril</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
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    <MAHolder>Elanco GmbH</MAHolder>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Salmonella typhimurium</ActiveSubstances>
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    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
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    <Territory>Northern Ireland</Territory>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-V</DistributionCategory>
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    <Name>Baytril Max 100 mg/ml Solution for Injection for Cattle and Pigs</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Enrofloxacin</ActiveSubstances>
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    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5096</VMNo>
    <DateOfIssue>2010-01-08</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <VMDProductNo>A010808</VMDProductNo>
    <Name>MilbeVet 12.5 mg/125 mg Chewable Tablets for Dogs </Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5097</VMNo>
    <DateOfIssue>2021-03-25</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
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    <UKPAR_Link />
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A010809</VMDProductNo>
    <Name>MilbeVet 2.5 mg/25 mg Chewable Tablets for Small Dogs and Puppies </Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Limited&lt;/span&gt;</Distributors>
    <VMNo>52127/5098</VMNo>
    <DateOfIssue>2021-03-25</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Milbemycin Oxime (A3 and A4), Praziquantel</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Chewable tablet</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_2530287.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_2141791.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A006954</VMDProductNo>
    <Name>AviPro ND C131 Lyophilisate for Suspension for Chickens and Turkeys</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5099 </VMNo>
    <DateOfIssue>2007-08-22</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Newcastle disease virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens, Turkeys</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Lyophilisate for suspension</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_183061.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_1298785.PDF</UKPAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A007630</VMDProductNo>
    <Name>Fortekor Flavour 20 mg Tablets for Dogs </Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5100</VMNo>
    <DateOfIssue>2010-04-28</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Benazepril Hydrochloride</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Cardio Vascular ACE inhibitor</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_269868.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_294673.PDF</UKPAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A007625</VMDProductNo>
    <Name>Fortekor Flavour 5 mg Tablets for Cats and Dogs</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5101</VMNo>
    <DateOfIssue>2010-04-28</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Benazepril Hydrochloride</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Tablet</PharmaceuticalForm>
    <TherapeuticGroup>Cardio Vascular ACE inhibitor</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_269865.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_294673.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_295978.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A006970</VMDProductNo>
    <Name>Fasinex 240, 240 mg/ml Oral Suspension for Cattle</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5102</VMNo>
    <DateOfIssue>2008-08-05</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Triclabendazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic flukicide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_221928.PDF</SPC_Link>
    <UKPAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_279995.PDF</UKPAR_Link>
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_261032.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A002862</VMDProductNo>
    <Name>Combinex Oral Suspension</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5103</VMNo>
    <DateOfIssue>1991-08-13</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Levamisole Hydrochloride, Triclabendazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Sheep</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral suspension</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic flukicide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_95647.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_539504.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A001831</VMDProductNo>
    <Name>Baytril 100 mg/ml Solution for use in Drinking Water for Chickens, Turkeys and Rabbits</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5104</VMNo>
    <DateOfIssue>1993-11-11</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Enrofloxacin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens, Rabbits, Turkeys</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for use in drinking water</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_112756.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_526261.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A009820</VMDProductNo>
    <Name>Seresto Flea and Tick Control 1.25 g + 0.56 g, Collar for Cats</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco GmbH&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5105</VMNo>
    <DateOfIssue>2017-09-04</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Flumethrin, Imidacloprid</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats</TargetSpecies>
    <DistributionCategory>NFA-VPS</DistributionCategory>
    <PharmaceuticalForm>Collar</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_1244135.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_1482895.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A009821</VMDProductNo>
    <Name>Seresto Flea and Tick Control 1.25 g + 0.56 g, Collar for Small Dogs ≤ 8 kg	</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd.&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5106</VMNo>
    <DateOfIssue>2017-09-04</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Flumethrin, Imidacloprid</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>NFA-VPS</DistributionCategory>
    <PharmaceuticalForm>Collar</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_1244229.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_1482897.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A009822</VMDProductNo>
    <Name>Seresto Flea and Tick Control 4.50 g + 2.03 g, Collar for Large Dogs &gt; 8 kg	</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco Europe Ltd.&lt;/span&gt;&lt;br /&gt;&lt;br /&gt;&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5107</VMNo>
    <DateOfIssue>2017-09-04</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Flumethrin, Imidacloprid</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>NFA-VPS</DistributionCategory>
    <PharmaceuticalForm>Collar</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_1244300.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_1482901.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A006265</VMDProductNo>
    <Name>Flubenvet 5 % w/w Premix for Medicated Feeding Stuff</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5108</VMNo>
    <DateOfIssue>2000-09-17</DateOfIssue>
    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Flubendazole</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Chickens, Goose, Partridge, Pheasants, Turkeys</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Premix for medicated feeding stuff</PharmaceuticalForm>
    <TherapeuticGroup>Anthelmintic</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_139295.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_546599.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A000399</VMDProductNo>
    <Name>Baytril 25 mg/ml Solution for Injection</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5119</VMNo>
    <DateOfIssue>1992-04-22</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Enrofloxacin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Dogs, Ornamental Birds, Pigs, Rabbits, Reptiles, Rodents</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_116001.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_526357.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A000398</VMDProductNo>
    <Name>Baytril 50 mg/ml Solution for Injection</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5120</VMNo>
    <DateOfIssue>1992-04-22</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Enrofloxacin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cats, Cattle, Dogs, Goats, Pigs, Sheep</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_117659.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_526411.PDF</PAAR_Link>
  </CurrentAuthorisedProducts>
  <CurrentAuthorisedProducts>
    <VMDProductNo>A001827</VMDProductNo>
    <Name>Baytril 100 mg/ml Solution for Injection</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5121</VMNo>
    <DateOfIssue>1993-11-11</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Enrofloxacin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Goats, Pigs, Sheep</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_116856.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_526282.PDF</PAAR_Link>
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  <CurrentAuthorisedProducts>
    <VMDProductNo>A001463</VMDProductNo>
    <Name>Tylan Soluble Powder for Oral Solution</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5122</VMNo>
    <DateOfIssue>1993-05-25</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Tylosin Tartrate</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle, Chickens, Pigs, Turkeys</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Powder for oral solution</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_140142.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_583510.PDF</PAAR_Link>
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    <VMDProductNo>A006153</VMDProductNo>
    <Name>Advantix 100 mg + 500 mg Spot-on Solution for Dogs (&gt; 4 kg ≤ 10 kg)</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5123</VMNo>
    <DateOfIssue>2003-12-23</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Imidacloprid, Permethrin (Cis:Trans 40:60)</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_110673.PDF</SPC_Link>
    <UKPAR_Link />
    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_513972.PDF</PAAR_Link>
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    <VMDProductNo>A006154</VMDProductNo>
    <Name>Advantix 250 mg + 1250 mg Spot-on Solution for Dogs (&gt; 10 kg ≤ 25 kg)</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5124</VMNo>
    <DateOfIssue>2003-12-23</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Imidacloprid, Permethrin (Cis:Trans 40:60)</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_110674.PDF</SPC_Link>
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    <PAAR_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_513895.PDF</PAAR_Link>
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    <VMDProductNo>A006152</VMDProductNo>
    <Name>Advantix 40 mg + 200 mg Spot-on Solution for Dogs (≤ 4 kg)</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5125</VMNo>
    <DateOfIssue>2003-12-23</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Imidacloprid, Permethrin (Cis:Trans 40:60)</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Spot-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
    <SPC_Link>https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_110672.PDF</SPC_Link>
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    <VMDProductNo>A006155</VMDProductNo>
    <Name>Advantix 400 mg + 2000 mg Spot-on Solution for Dogs (&gt; 25 kg ≤ 40 kg)</Name>
    <MAHolder>Elanco GmbH</MAHolder>
    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
    <VMNo>52127/5126</VMNo>
    <DateOfIssue>2003-12-23</DateOfIssue>
    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Great Britain</Territory>
    <ActiveSubstances>Imidacloprid, Permethrin (Cis:Trans 40:60)</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Dogs</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
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    <ControlledDrug>N</ControlledDrug>
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    <Name>Advantage 40 Spot-on Solution for Dogs</Name>
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    <Distributors>&lt;span&gt;Elanco UK AH Ltd&lt;/span&gt;</Distributors>
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    <Name>Flyclanil 5% Pour-on Suspension for Sheep</Name>
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    <ActiveSubstances>Infectious bursal disease virus</ActiveSubstances>
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    <DateOfIssue>2018-08-21</DateOfIssue>
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    <Name>Vanguard CPV Suspension for Injection</Name>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <Name>Vanguard Lepto ci</Name>
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    <Distributors>&lt;span&gt;Zoetis UK Limited&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National</AuthorisationRoute>
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    <ActiveSubstances>Leptospira canicola, Leptospira icterohaemorrhagiae</ActiveSubstances>
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    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
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    <MAHolder>Zoetis Belgium S.A.</MAHolder>
    <Distributors>&lt;span&gt;Downland Marketing Limited&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>National (Informed Consent)</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Moxidectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Sheep</TargetSpecies>
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    <PharmaceuticalForm>Oral solution</PharmaceuticalForm>
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    <Distributors>&lt;span&gt;Downland Marketing Limited&lt;/span&gt;</Distributors>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Moxidectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <Name>Versifel CVR</Name>
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    <AuthorisationRoute>National</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Feline calicivirus, Feline panleukopenia virus, Feline viral rhinotracheitis virus</ActiveSubstances>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Powder and solvent for solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
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    <Name>Zermasect Sheep Pour-on Alphacypermethrin 12.5 g/l Pour-on Solution</Name>
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    <ActiveSubstances>Alpha-Cypermethrin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Pour-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Ectoparasiticide</TherapeuticGroup>
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    <Name>Zermex 20 mg/ml LA Solution for Injection for Sheep</Name>
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    <Distributors>&lt;span&gt;Zoetis Belgium S.A.&lt;/span&gt;</Distributors>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Moxidectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Sheep</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <Name>Synulox Lactating Cow Intramammary Suspension</Name>
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    <Distributors>&lt;span&gt;Zoetis Belgium S.A.&lt;/span&gt;</Distributors>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Amoxicillin, Clavulanic Acid, Prednisolone</ActiveSubstances>
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    <Name>Versiguard Rabies Suspension for Injection</Name>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Rabies virus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <Name>CIDR 1.38 g Vaginal Delivery System for Cattle</Name>
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    <Name>CIDR OVIS 0.35 g Vaginal Delivery System for Sheep</Name>
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    <Distributors>&lt;span&gt;Zoetis Belgium S.A.&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Progesterone</ActiveSubstances>
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    <ActiveSubstances>Bovine parainfluenza virus 3, Bovine respiratory syncytial virus, Bovine viral diarrhoea virus</ActiveSubstances>
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    <TherapeuticGroup>Neurological Agent general anaesthetic</TherapeuticGroup>
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    <ActiveSubstances>Infectious bovine rhinotraceitis virus</ActiveSubstances>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Powder and solvent for solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Live Viral Vaccine</TherapeuticGroup>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Suspension for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
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    <ActiveSubstances>Mycoplasma hyopneumoniae</ActiveSubstances>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Emulsion for injection</PharmaceuticalForm>
    <TherapeuticGroup>Inactivated Bacterial Vaccine</TherapeuticGroup>
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    <Name>Versican Plus BbPi IN Nasal Drops, Lyophilisate and Solvent for Suspension for Dogs </Name>
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    <Name>Rispoval IBR-Marker Inactivated Suspension for Injection for Cattle </Name>
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    <Name>Rispoval 2 / BRSV + Pi3 Lyophilisate and Solvent for Suspension for Injection for Cattle</Name>
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    <Distributors>&lt;span&gt;Zoetis Belgium S.A.&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Bovine parainfluenza virus 3, Bovine respiratory syncytial virus</ActiveSubstances>
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    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
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    <Name>Poulvac TRT Lyophilisate for Oculonasal Suspension for Turkeys</Name>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Avian pneumovirus</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
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    <PharmaceuticalForm>Lyophilisate for oculonasal suspension</PharmaceuticalForm>
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    <Distributors>&lt;span&gt;Zoetis UK Limited&lt;/span&gt;</Distributors>
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    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Moxidectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Sheep</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Oral solution</PharmaceuticalForm>
    <TherapeuticGroup>Endectocide</TherapeuticGroup>
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    <Name>Cydectin 0.5% w/v Pour-on for Cattle</Name>
    <MAHolder>Zoetis Belgium S.A.</MAHolder>
    <Distributors>&lt;span&gt;Zoetis UK Limited&lt;/span&gt;</Distributors>
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    <Territory>Northern Ireland</Territory>
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    <ControlledDrug>N</ControlledDrug>
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    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Pour-on solution</PharmaceuticalForm>
    <TherapeuticGroup>Endectocide</TherapeuticGroup>
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    <Name>Cydectin 10% LA Solution for Injection for Cattle</Name>
    <MAHolder>Zoetis Belgium S.A.</MAHolder>
    <Distributors>&lt;span&gt;Zoetis UK Limited&lt;/span&gt;</Distributors>
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    <AuthorisationRoute>Mutually Recognised</AuthorisationRoute>
    <Territory>Northern Ireland</Territory>
    <ActiveSubstances>Moxidectin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-VPS</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Endectocide</TherapeuticGroup>
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    <Name>Cydectin 20 mg/ml LA Solution for Injection for Sheep</Name>
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    <Distributors>&lt;span&gt;Zoetis UK Limited&lt;/span&gt;</Distributors>
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    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Endectocide</TherapeuticGroup>
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    <Name>Cydectin TriclaMox 1 mg/ml + 50 mg/ml Oral Solution for Sheep</Name>
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    <Distributors>&lt;span&gt;Zoetis UK Limited&lt;/span&gt;</Distributors>
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    <DistributionCategory>POM-VPS</DistributionCategory>
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    <Distributors>&lt;span&gt;Zoetis UK Limited&lt;/span&gt;</Distributors>
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    <Name>Draxxin Plus 100 mg/ml + 120 mg/ml Solution for Injection for Cattle</Name>
    <MAHolder>Zoetis Belgium S.A.</MAHolder>
    <Distributors>&lt;span&gt;Zoetis UK Limited&lt;/span&gt;</Distributors>
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    <ActiveSubstances>Ketoprofen, Tulathromycin</ActiveSubstances>
    <ControlledDrug>N</ControlledDrug>
    <TargetSpecies>Cattle</TargetSpecies>
    <DistributionCategory>POM-V</DistributionCategory>
    <PharmaceuticalForm>Solution for injection</PharmaceuticalForm>
    <TherapeuticGroup>Antimicrobial; Anti Inflammatory</TherapeuticGroup>
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    <Name>Poulvac AE Lyophilisate for Use in Drinking Water for Chickens</Name>
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    <Distributors>&lt;span&gt;Zoetis UK Limited&lt;/span&gt;</Distributors>
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    <Distributors>&lt;span&gt;Zoetis Belgium S.A.&lt;/span&gt;</Distributors>
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    <VMDProductNo>A014203</VMDProductNo>
    <Name>Poulvac NDW </Name>
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    <VMNo>60021/3081</VMNo>
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    <Name>Synulox Palatable Tablets 40 mg/10 mg </Name>
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    <Name>Ivomec Super Injection for Cattle (Ivermectin and Clorsulon)	</Name>
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