Open regulatory directory
Veterinary drug regulators and official product registers
A country-by-country verification directory for canine longevity drug claims. It identifies the regulator and public register that should answer the legal-status question before an announcement, seller page, foreign approval, or technical milestone is described as local availability.
Last reviewed August 1, 2026 · CC BY 4.0 with attribution
| Country | Veterinary regulator | Official register | Current Atlas classification | Guide |
|---|---|---|---|---|
| United States (US) | U.S. Food and Drug Administration Center for Veterinary Medicine (FDA CVM) | Animal Drugs @ FDA | Development milestones reported; approval not verified | Evidence pack |
| Canada (CA) | Health Canada Veterinary Drugs Directorate (VDD) | Drug Product Database | No Canadian authorization verified | Evidence pack |
| United Kingdom (GB) | Veterinary Medicines Directorate (VMD) | VMD Product Information Database | No UK marketing authorisation verified | Evidence pack |
| Australia (AU) | Australian Pesticides and Veterinary Medicines Authority (APVMA) | APVMA PubCRIS | No Australian registration verified | Evidence pack |
| New Zealand (NZ) | Ministry for Primary Industries (MPI), Agricultural Compounds and Veterinary Medicines (ACVM) | ACVM register | No New Zealand registration verified | Evidence pack |
What this directory can establish
- · Which national authority regulates veterinary medicines in the covered market.
- · Which official product database or register should be searched.
- · Which country-specific guide documents the current Atlas classification and sources.
- · When the regulator pack was last reviewed.
What it cannot establish alone
- · That a named product is approved, registered, marketed, importable, or in stock.
- · That a foreign approval or development milestone applies locally.
- · That a dog matches an approved label or is clinically eligible.
- · That a supplement, trial, permit, special-access pathway, and approved drug are equivalent.
Reproducible verification workflow
- 1. Identify the jurisdiction.
Do not infer local status from the location of a sponsor, trial, pharmacy, or media outlet. - 2. Search the official register.
Use the exact product, active ingredient, sponsor, and application or registration number when available. - 3. Open the legal record and label.
Confirm status, species, indication, population, dose, warnings, dates, and holder. - 4. Preserve the evidence boundary.
Record whether the source proves authorization, commercial supply, trial access, or only a development milestone.
Educational directory only. Recheck official records and consult a licensed veterinarian for current legal and clinical decisions.