France· FR:69171174
RAPAMUNE 0,5 mg, comprimé enrobé
A medicinal product containing sirolimus, registered in France by PFIZER EUROPE MA EEIG (BELGIQUE), on the national reimbursement list.
Checked against Base de données publique des médicaments — BDPM (France) on
Informational only — not a medical device.
The record
At a glance
Base de données publique des médicaments — BDPM (France)- Active substance
- SIROLIMUS
- Manufacturer
- PFIZER EUROPE MA EEIG (BELGIQUE)
- Country
- France (FR)
- ATC code
- —
- Reimbursed
- Yes
- Source register
- Base de données publique des médicaments — BDPM (France)
- Last checked
- September 12, 2026
Packs & prices · 1
1 priced- cip133400949304578plaquette(s) thermoformée(s) PVC polyéthylène aluminium-ACLAR de 30 comprimé(s)EUR 49.39
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Sirolimus in 16 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaRAPAMUNEPfizer Europe MA EEIG, Bruxelles
- SwitzerlandRapamune 0.5 mg, überzogene TablettenPfizer AG
- BelgiumRapamune 0.5 mgPfizer Europe MA
- FinlandRapamunePfizer Europe MA EEIG
- IrelandRapamune 0.5 mg Coated tabletPfizer Europe MA EEIG
- NetherlandsRapamune 0,5 mg omhulde tablettenPfizer Europe MA EEIG
- SpainRAPAMUNE 0,5 mg COMPRIMIDOS RECUBIERTOSPfizer Europe Ma Eeig
- United StatesFYARROAadi Bioscience, Inc.
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- Germany · Sirolimus Panacea Biotec
- Iceland · Hyftor, Rapamune
- Liechtenstein · Hyftor, Rapamune
- Norway · Hyftor, Rapamune
Source: European Medicines Agency, Article 57 product data.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of Base de données publique des médicaments — BDPM (France). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.
For developers
The same record over the API, and the raw payload
GET /v1/drugs/e1e410ec-a8ae-436c-b8df-ca245a54a875 GET /v1/drugs/e1e410ec-a8ae-436c-b8df-ca245a54a875?format=fhir
Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.
{
"cis": "69171174",
"date_amm": "2010-07-06",
"type_amm": "Procédure centralisée",
"numero_ue": "EU/1/01/171",
"substance": "SIROLIMUS",
"statut_amm": "Autorisation active",
"statut_bdm": null,
"forme_pharmaceutique": "comprimé enrobé",
"voies_administration": "orale",
"etat_commercialisation": "Commercialisée",
"surveillance_renforcee": "Non"
}See everything about sirolimus.
This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.