France· FR:67503464
TRANSLARNA 125 mg, granulés pour suspension buvable
A ataluren product containing ataluren, registered in France by PTC THERAPEUTICS INTERNATIONAL (IRLANDE). The same ATC class is registered in 6 of our 19 countries.
Checked against Base de données publique des médicaments — BDPM (France) on
Informational only — not a medical device.
Where it is registered
Ataluren is registered in 6 of 19 countries.
Countries holding a registration under ATC M09AX03 (ataluren), each read from that country’s own register.
- This record: France, from Base de données publique des médicaments — BDPM (France)
- 4 of them publish a price we can compare per daily dose
Ataluren · ATC M09AX03
6 / 19 countries
- Belgiumprice
- Finlandprice
- Franceprice
- Ireland
- Polandprice
- United Kingdom
The record
At a glance
Base de données publique des médicaments — BDPM (France)- Active substance
- ATALUREN
- Manufacturer
- PTC THERAPEUTICS INTERNATIONAL (IRLANDE)
- Country
- France (FR)
- ATC code
- M09AX03
- ATC class
- Ataluren
- Defined daily dose
- 2.8 g, O
- Reimbursed
- No
- Source register
- Base de données publique des médicaments — BDPM (France)
- Last checked
- September 12, 2026
Packs & prices · 1
- cip13340092795914130 sachet(s) aluminium
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Ataluren in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SpainTRANSLARNA 125 MG GRANULADO PARA SUSPENSION ORALPtc Therapeutics International Limited
- FinlandTranslarnaPTC Therapeutics International Limited
- PolandTranslarnaPTC Therapeutics International Limited
- BelgiumTranslarna 1000 mgPTC Therapeutics
- United KingdomTranslarna 1,000mg granules for oral suspension sachetsPTC Therapeutics Ltd
- IrelandTranslarnaPTC Therapeutics International Limited
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/e404bdaa-998e-4b5f-974a-45406680e22b GET /v1/drugs/e404bdaa-998e-4b5f-974a-45406680e22b?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": "67503464",
"date_amm": "2014-07-31",
"type_amm": "Procédure centralisée",
"numero_ue": "EU/1/13/902",
"substance": "ATALUREN",
"atc_source": "fr_atc_restore_2026-09-06",
"statut_amm": "Autorisation archivée",
"statut_bdm": "Alerte",
"forme_pharmaceutique": "granulés pour suspension buvable",
"voies_administration": "orale",
"etat_commercialisation": "Non commercialisée",
"surveillance_renforcee": "Non"
}See everything about ataluren.
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.