France· FR:64424905
BEMFOLA 150 UI/0,25 ml, solution injectable en stylo prérempli
A medicinal product containing follitropine alfa, registered in France by GEDEON RICHTER ( HONGRIE), 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
- FOLLITROPINE ALFA
- Manufacturer
- GEDEON RICHTER ( HONGRIE)
- 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- cip1334009279391501 cartouche(s) en verre de 0,25 ml dans1 stylo pré-rempli avec 1 aiguille(s) avec tampon(s) alcoolisé(s)EUR 29.39
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Follitropine alfa in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- NetherlandsBemfola 150 IE/0,25 ml oplossing voor injectie in een voorgevulde penGedeon Richter Plc.
- IrelandOvaleap 300 IU/0.5 mL solution for injectionTheramex Ireland Limited
- United KingdomBemfola 150units/0.25ml solution for injection pre-filled pensGedeon Richter (UK) Ltd
- CzechiaBEMFOLAGedeon Richter Plc., Budapešť
- SpainBEMFOLA 150 UI/0,25 ml solucion inyectable en pluma precargadaGedeon Richter Plc.
- FinlandBemfolaAbacus Medicine A/S
- BelgiumBemfola 150 IU/0.25 mlGedeon Richter
- ItalyBEMFOLA*1 cartuccia in penna preriempita SC 150 UI/0,25 ml + agoGEDEON RICHTER PLC
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Bemfola, Gonal-F
- Liechtenstein · Bemfola, Gonal-F
- Norway · Bemfola, Gonal-F
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/e397f793-1f79-4848-8edb-bb2c041dcaf0 GET /v1/drugs/e397f793-1f79-4848-8edb-bb2c041dcaf0?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": "64424905",
"date_amm": "2014-03-27",
"type_amm": "Procédure centralisée",
"numero_ue": "EU/1/13/909",
"substance": "FOLLITROPINE ALFA",
"statut_amm": "Autorisation active",
"statut_bdm": null,
"forme_pharmaceutique": "solution injectable",
"voies_administration": "sous-cutanée",
"etat_commercialisation": "Commercialisée",
"surveillance_renforcee": "Non"
}See everything about follitropine alfa.
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.