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France· FR:68343525

KISQALI 200 mg, comprimé pelliculé

A medicinal product containing succinate de ribociclib, registered in France by NOVARTIS EUROPHARM (IRLANDE), 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…normalisedKISQALI 200 mg, comprimé pelliculéATC—REGISTER NO.FR:68343525PACKS LISTED6CHECKEDSeptember 12, 2026

The record

At a glance

Base de données publique des médicaments — BDPM (France)
Active substance
SUCCINATE DE RIBOCICLIB
Manufacturer
NOVARTIS EUROPHARM (IRLANDE)
Country
France (FR)
ATC code
—
Reimbursed
Yes
Source register
Base de données publique des médicaments — BDPM (France)
Last checked
September 12, 2026

Packs & prices · 6

6 priced
  • cip13
    3400930109335
    plaquette(s) polychlortrifluoroéthylène PVC de 21 comprimé(s)
    EUR 852.13
  • cip13
    3400930109342
    plaquette(s) polychlortrifluoroéthylène PVC de 42 comprimé(s)
    EUR 1.67
  • cip13
    3400930109359
    plaquette(s) polychlortrifluoroéthylène PVC de 63 comprimé(s)
    EUR 2.47
  • cip13
    3400930323434
    plaquette(s) polyamide aluminium PVC de 21 comprimé(s)
    EUR 851.48
  • cip13
    3400930323441
    plaquette(s) polyamide aluminium PVC de 42 comprimé(s)
    EUR 1.67
  • cip13
    3400930323458
    plaquette(s) polyamide aluminium PVC de 63 comprimé(s)
    EUR 2.47

Regulatory notes

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

Same medicine, other countries

Succinate de ribociclib in 14 other countries

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

All succinate de ribociclib products

Authorised across Europe · EMA

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

  • Iceland · Kisqali
  • Liechtenstein · Kisqali
  • Norway · Kisqali

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/ac73a88a-e5a3-4549-bb3f-54cb378d6489
GET /v1/drugs/ac73a88a-e5a3-4549-bb3f-54cb378d6489?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": "68343525",
  "date_amm": "2017-08-22",
  "type_amm": "Procédure centralisée",
  "numero_ue": "EU/1/17/1221",
  "substance": "SUCCINATE DE RIBOCICLIB",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "comprimé pelliculé",
  "voies_administration": "orale",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Non"
}

See everything about succinate de ribociclib.

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.