Veterinary medicine packages
Veterinary medicine packages from the BVL reporting dataset.
- Records
- 3,691
- Licence
- Publisher terms
BVL pack IDRegistration numberUPD UUID
🇩🇪 Germany · EMA · BVL · Paul-Ehrlich-Institut
Search the medicines authorised in Germany as reported to the European Medicines Agency, centrally authorised medicines with ATC codes, and veterinary medicines from BVL and the Paul-Ehrlich-Institut. One REST API, collected daily, with the source and licence of every record.
Instant access. No credit card required.
curl -G https://api.medifontis.com/v1/drugs \
-H "Authorization: Bearer mf_live_your_api_key" \
--data-urlencode "country=de" \
--data-urlencode "q=ozempic"const params = new URLSearchParams({ country: 'de', q: 'ozempic' })
const response = await fetch(`https://api.medifontis.com/v1/drugs?${params}`, {
headers: { Authorization: 'Bearer mf_live_your_api_key' },
})
if (!response.ok) throw new Error(`Medifontis ${response.status}`)
const { results, nextOffset } = await response.json()import requests
response = requests.get(
"https://api.medifontis.com/v1/drugs",
params={"country": "de", "q": "ozempic"},
headers={"Authorization": "Bearer mf_live_your_api_key"},
timeout=10,
)
response.raise_for_status()
results = response.json()["results"]
{
"country": "de",
"results": [
{
"country": "de",
"sourceId": "de.ema.article57",
"id": "de:ema:article57:3f301c505c8d15200fcc",
"kind": "products",
"name": "Ozempic",
"names": [
"Ozempic",
"Semaglutide"
],
"identifiers": [],
"data": {
"name": "Ozempic",
"holder": "Novo Nordisk A/S",
"useDomain": "unknown",
"databaseDate": "2026-10-09",
"listingStatus": "listed-as-authorised",
"sourceRowCount": 1
},
"retrievedAt": "2026-10-20T01:00:19.432Z",
"sourceUrl": "https://www.ema.europa.eu/en/documents/other/article-57-product-data_en.xlsx",
"licence": {
"id": "LicenseRef-EMA-Legal-Notice",
"attribution": "Source: European Medicines Agency (EMA), Article 57 product data (EMA/518502/2018), based on data submitted by marketing-authorisation holders."
}
}
],
"nextOffset": null
}
Try it before you integrate
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🇩🇪 Germany
Every record comes from one of these publishers, with its counts and licence as of the latest collection.
Veterinary medicine packages from the BVL reporting dataset.
BVL pack IDRegistration numberUPD UUID
Medicines authorised in Germany as reported to the European Medicines Agency under Article 57: product names, active substances and routes.
Medicines authorised through the EU centralised procedure, with EMA product numbers and ATC codes.
EMA product numberATC
Veterinary vaccines and immunological medicines authorised by the Paul-Ehrlich-Institut.
Registration number
Why Medifontis
Records from 199 countries share the same JSON shape, so code written for one country works for every other.
Search brand names, active ingredients and identifiers such as AIC, CN, CIP13, NDC, DIN or BNF codes, without worrying about accents or case.
Each result carries its source URL, retrieval time, licence and limitations, so you can show users exactly where the data comes from.
Filter by use domain and target species wherever the source publishes them.
A dedicated endpoint returns distinct names while users type, ranked exact, prefix, then substring.
Every source is collected on a daily schedule and published atomically, so you never read a half-imported country.
Provenance
Medifontis never invents or merges data. Each record keeps the identifiers its publisher assigned and states its source, licence and known limitations.
sourceUrl
links the official dataset the record was collected from.
retrievedAt
is when Medifontis collected it.
licence
names the publisher’s terms and the attribution to show.
limitations
lists what the source does not establish, such as current availability.
{
"sourceUrl": "https://www.ema.europa.eu/en/documents/other/article-57-product-data_en.xlsx",
"retrievedAt": "2026-10-20T01:00:19.432Z",
"licence": {
"id": "LicenseRef-EMA-Legal-Notice",
"url": "https://www.ema.europa.eu/en/about-us/legal-notice",
"scope": "rows of EMA’s public Article 57 product data authorised in Germany or centrally in the European Union",
"reviewedAt": "2026-09-29",
"attribution": "Source: European Medicines Agency (EMA), Article 57 product data (EMA/518502/2018), based on data submitted by marketing-authorisation holders.",
"documentsIncluded": false
},
"limitations": [
"Germany has no free, complete official bulk medicine database with PZNs: BfArM’s AMIce public search is interactive only, its § 31b reference database is supplied to commercial users on request, and the GKV-Spitzenverband and BfArM price lists are PDF-only for reasons of usage rights.",
"EMA’s Article 57 export names every medicinal product authorised in Germany (national, mutual-recognition and decentralised procedures) and every centrally authorised EU product, as submitted by marketing-authorisation holders; submissions can lag an authorisation change.",
"A record is one product name, active-substance text, route and marketing-authorisation holder. Strengths, forms, packs, PZNs, authorisation numbers and dates are not published, so rows EMA lists more than once for one such product are kept together with their count.",
"The export publishes no legal category (verschreibungspflichtig, apothekenpflichtig, freiverkäuflich), so the prescription classification stays unknown; listing is not proof of current authorisation, marketing, availability or reimbursement.",
"Active-substance names are the English xEVMPD names EMA publishes, not German INN spellings.",
"EMA’s legal notice permits commercial and non-commercial reproduction with acknowledgement of EMA as the source; its exception for third-party content leaves the status of holder-submitted text unconfirmed."
]
}
Use cases
Let clinicians find the exact authorised product and keep its national code with the prescription.
Match your catalogue to national codes and keep product names and holders in sync with the regulator.
Autocomplete medicine names in medication lists, reminders and intake forms.
Ground answers about medicines in official records instead of model memory.
Track authorised products, holders and presentations across countries.
Search veterinary medicines and their target species where regulators publish them.
Coverage
The same endpoints and the same record shape for every country Medifontis covers.
FAQ
From the official publishers listed above: EMA · BVL · Paul-Ehrlich-Institut. Medifontis collects each source as published and keeps every record independent; records from different sources are never merged or matched by name.
Each source is collected every day and the country is published atomically once collection succeeds. Every record carries the time it was retrieved from its source.
Names match anywhere in the text and identifiers match from their first character. For this country that covers EMA product numbers, ATC codes and registration numbers.
Yes, within the licence of each source. Every record includes its licence and attribution text, and some publishers restrict commercial redistribution, so check the licences of the sources you rely on.
No. Medifontis reports what official sources publish. It does not decide whether a medicine is suitable, available or reimbursed for a patient.
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