Amoxibactin 50 mg Tablets for Dogs and Cats

Veterinary medicine · Veterinary Medicines Directorate · United Kingdom

VMD product A011336
VM number 41821/4014

What the source publishes

Holder: Le Vet Beheer B.V.
Active ingredients: Amoxicillin
Form: Tablet
Administrative status: not-independently-verified
Supply regime: POM-V

Publisher documents

Summary of product characteristics

Names this record is found by

Complete source data

gb:vmd:products:A011336

{
  "form": "Tablet",
  "gtin": null,
  "name": "Amoxibactin 50 mg Tablets for Dogs and Cats",
  "holder": "Le Vet Beheer B.V.",
  "routes": [],
  "smpcUrl": "https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_697208.PDF",
  "marketed": null,
  "strength": null,
  "vmNumber": "41821/4014",
  "packageId": null,
  "productId": "A011336",
  "territory": "Northern Ireland",
  "useDomain": "veterinary",
  "nativeRecord": {
    "fields": {
      "Name": "Amoxibactin 50 mg Tablets for Dogs and Cats",
      "VMNo": "41821/4014",
      "MAHolder": "Le Vet Beheer B.V.",
      "SPC_Link": "https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_697208.PDF",
      "PAAR_Link": "https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_890645.PDF",
      "Territory": "Northern Ireland",
      "UKPAR_Link": "https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_1981836.PDF",
      "DateOfIssue": "2014-12-17",
      "Distributors": "<span>Dechra Veterinary Products Limited</span>",
      "VMDProductNo": "A011336",
      "TargetSpecies": "Cats, Dogs",
      "ControlledDrug": "N",
      "ActiveSubstances": "Amoxicillin",
      "TherapeuticGroup": "Antimicrobial",
      "AuthorisationRoute": "Mutually Recognised",
      "PharmaceuticalForm": "Tablet",
      "DistributionCategory": "POM-V"
    },
    "category": "CurrentAuthorisedProducts",
    "catalogueUrl": "https://www.vmd.defra.gov.uk/ProductInformationDatabase/downloads/VMD_ProductInformationDatabase.xml"
  },
  "sourceStatus": "CurrentAuthorisedProducts",
  "supplyRegime": "POM-V",
  "targetSpecies": [
    {
      "code": null,
      "label": "Cats",
      "native": {
        "field": "TargetSpecies",
        "label": "Cats",
        "value": "Cats, Dogs"
      },
      "sourceId": "gb.vmd.product-information",
      "population": "Cats",
      "canonicalId": "cat",
      "mappingStatus": "mapped",
      "mappingVersion": 1
    },
    {
      "code": null,
      "label": "Dogs",
      "native": {
        "field": "TargetSpecies",
        "label": "Dogs",
        "value": "Cats, Dogs"
      },
      "sourceId": "gb.vmd.product-information",
      "population": "Dogs",
      "canonicalId": "dog",
      "mappingStatus": "mapped",
      "mappingVersion": 1
    }
  ],
  "sourceCategory": "CurrentAuthorisedProducts",
  "sourceDocuments": [
    {
      "field": "SPC_Link",
      "linkScope": "source-product-document",
      "sourceUrl": "https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_697208.PDF",
      "bodyCollected": false
    },
    {
      "field": "UKPAR_Link",
      "linkScope": "source-product-document",
      "sourceUrl": "https://www.vmd.defra.gov.uk/productinformationdatabase/files/UKPAR_Documents/UKPAR_1981836.PDF",
      "bodyCollected": false
    },
    {
      "field": "PAAR_Link",
      "linkScope": "source-product-document",
      "sourceUrl": "https://www.vmd.defra.gov.uk/productinformationdatabase/files/PAA_Documents/PAA_890645.PDF",
      "bodyCollected": false
    }
  ],
  "sourceIssueDate": "2014-12-17",
  "territoryStatus": "reported",
  "activeSubstances": "Amoxicillin",
  "therapeuticGroup": "Antimicrobial",
  "useDomainEvidence": {
    "basis": "publisher-veterinary-register-scope",
    "field": "VMD_PIDProducts/category",
    "value": "CurrentAuthorisedProducts",
    "version": 1,
    "sourceId": "gb.vmd.product-information"
  },
  "withdrawalPeriods": [],
  "authorisationRoute": "Mutually Recognised",
  "nativeRecordSha256": "380be99d384f41d6254d99ab85c14beddb1d0f1cc83644bb1b0309b81df5c851",
  "packageDescription": null,
  "patientEligibility": "not-assessed",
  "targetSpeciesStatus": "reported",
  "administrativeStatus": "not-independently-verified",
  "prescriptionCategory": "unknown",
  "sourceControlledDrug": "N",
  "sourceExpirationDate": null,
  "sourceSuspensionDate": null,
  "distributorsSourceHtml": "<span>Dechra Veterinary Products Limited</span>",
  "withdrawalPeriodsStatus": "not-reported"
}

Veterinary medicines

Contains public sector information licensed under the Open Government Licence v3.0. Source: Veterinary Medicines Directorate, Product Information Database. Export metadata normalized by Medifontis; no endorsement implied.

Retrieved: November 10, 2026
Licence: Open Government Licence v3.0
Source id: gb.vmd.product-information

Official source

What this source does not establish

Complete chosen four-category official PID export, not all possible historical authorisations, refused applications or independent product-detail facts. Every whole UK publication also requires gb.mhra.products and gb.nhsbsa.bnf-snomed.
Great Britain, Northern Ireland and United Kingdom territory values remain distinct; seven baseline homeopathic entries and one reviewed current authorisation (A014157, in exports since 22 October 2026) report no territory, which stays unreported. UK country code gb never broadens a territorial authorisation. Aligned entries and shared VM numbers are not merged.
VMDProductNo is the publisher product key, not a pack or GTIN. VMNo is a literal source authorisation/registration reference; EU ranges are retained without inventing package identities.
No structured pack identifiers, package sizes, ingredient amounts, strength, administration routes or withdrawal periods are published by the selected exports. Native form, species/populations, distribution categories, controlled-drug and dates remain source facts, not clinical defaults or prescribing eligibility.
Source category is retained as the publisher listing status. Current marketing, dispensing permission, availability and patient suitability are unverified. Homeopathic registration does not establish efficacy.
All native XML/XLSX fields and whole originals are retained. Product-detail pages additionally expose product-literature links, previous VM numbers and alignment/UMA facts; these are not in the selected export and are not claimed as collected.
Official source document links are retained only. Some SPC_Link values are generic EMA UPD information links, not product-specific SPC documents; source-information-link marks that distinction. No document content is copied.
PID site footer declares Crown copyright and OGL v3.0 except where otherwise stated. This metadata use does not establish a grant for third-party document bodies, publisher endorsement or clinical permission.

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