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France· FR:62624259

LITFULO 50 mg, gélule

A ritlecitinib product containing tosylate de ritlécitinib, registered in France by PFIZER EUROPE MA EEIG (BELGIQUE), on the national reimbursement list. The same ATC class is registered in 16 of our 19 countries.

Reimbursed in France (Assurance maladie)ATC L04AF08

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…normalisedLITFULO 50 mg, géluleATCL04AF08REGISTER NO.FR:62624259PACKS LISTED1CHECKEDSeptember 12, 2026

Where it is registered

Ritlecitinib is registered in 16 of 19 countries.

Countries holding a registration under ATC L04AF08 (ritlecitinib), each read from that country’s own register.

  • This record: France, from Base de données publique des médicaments — BDPM (France)
  • 10 of them publish a price we can compare per daily dose

Ritlecitinib · ATC L04AF08

16 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Japan
  • Netherlands
  • Norwayprice
  • Polandprice
  • Spainprice
  • Switzerlandprice
  • United Kingdom
  • United Statesprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

Base de données publique des médicaments — BDPM (France)
Active substance
TOSYLATE DE RITLÉCITINIB
Manufacturer
PFIZER EUROPE MA EEIG (BELGIQUE)
Country
France (FR)
ATC code
L04AF08
ATC class
Ritlecitinib
Defined daily dose
50 mg, O
Reimbursed
Yes
Source register
Base de données publique des médicaments — BDPM (France)
Last checked
September 12, 2026

Packs & prices · 1

1 priced
  • cip13
    3400930279724
    plaquette(s) OPA : polyamide orienté aluminium PVC-Aluminium de 30 gélule(s)
    EUR 971.74

Regulatory notes

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

Same medicine, other countries

Ritlecitinib in 14 other countries

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

All ritlecitinib products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • Iceland · Litfulo
  • Liechtenstein · Litfulo
  • Norway · Litfulo

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/862beb83-23d1-478f-b2dd-b048366aad3e
GET /v1/drugs/862beb83-23d1-478f-b2dd-b048366aad3e?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": "62624259",
  "date_amm": "2023-09-15",
  "type_amm": "Procédure centralisée",
  "numero_ue": "EU/1/23/1755",
  "substance": "TOSYLATE DE RITLÉCITINIB",
  "atc_source": "fr_atc_restore_2026-09-06",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "gélule",
  "voies_administration": "orale",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Oui"
}

See everything about ritlecitinib.

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.