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France· FR:65407392

BEXAROTENE CIPLA 75 mg, capsule molle

A medicinal product containing bexarotène, registered in France by CIPLA EUROPE (BELGIQUE), on the national reimbursement list.

Reimbursed in France (Assurance maladie)

Checked against Base de données publique des médicaments — BDPM (France) on

Informational only — not a medical device.

SOURCE REGISTER · FRBase de données publique des médicament…normalisedBEXAROTENE CIPLA 75 mg, capsule molleATC—REGISTER NO.FR:65407392PACKS LISTED1CHECKEDSeptember 12, 2026

The record

At a glance

Base de données publique des médicaments — BDPM (France)
Active substance
BEXAROTÈNE
Manufacturer
CIPLA EUROPE (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
  • cip13
    3400930241172
    1 flacon polyéthylène haute densité (PEHD) avec fermeture de sécurité enfant de 100 capsules
    EUR 292.81

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Bexarotène in 14 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All bexarotène products

Authorised across Europe · EMA

The same active substance is authorised in 11 EEA countries. Names it is sold under:

  • Austria · Bexagia
  • Germany · Bexaroten Cipla
  • Denmark · Bexarotene
  • Spain · Bexaroteno Cipla
  • Finland · Bexarotene Amdipharm
  • United Kingdom (Northern Ireland) · Bexarotene Genus Pharmaceuticals Ltd.
  • Iceland · Targretin
  • Italy · Bexarotene Cipla
  • Liechtenstein · Targretin
  • Norway · Bexarotene Amdipharm, Targretin
  • Sweden · Bexarotene Amdipharm

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/bb4df1ee-e686-4eac-bba8-fcec73cb3a27
GET /v1/drugs/bb4df1ee-e686-4eac-bba8-fcec73cb3a27?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": "65407392",
  "date_amm": "2021-10-27",
  "type_amm": "Procédure décentralisée",
  "numero_ue": null,
  "substance": "BEXAROTÈNE",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "capsule molle",
  "voies_administration": "orale",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Non"
}

See everything about bexarotène.

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.