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France· FR:66498605

FLUOSTEROL 0,25 mg/800 U.I./dose, solution buvable

A medicinal product containing fluorure de sodium + concentrat de cholécalciférol, forme pulvérulente, registered in France by CRINEX, 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…normalisedFLUOSTEROL 0,25 mg/800 U.I./dose, sol…ATC—REGISTER NO.FR:66498605PACKS LISTED1CHECKEDSeptember 12, 2026

The record

At a glance

Base de données publique des médicaments — BDPM (France)
Active substance
FLUORURE DE SODIUM + CONCENTRAT DE CHOLÉCALCIFÉROL, FORME PULVÉRULENTE
Manufacturer
CRINEX
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
    3400935718495
    1 flacon(s) polyéthylène avec fermeture de sécurité enfant de 22,5 ml avec seringue(s) pour administration orale polyéthylène polystyrène
    EUR 2.54

Regulatory notes

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

Same medicine, other countries

Fluorure de sodium + concentrat de cholécalciférol, forme pulvérulente in 2 other countries

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

All fluorure de sodium + concentrat de cholécalciférol, forme pulvérulente products

Authorised across Europe · EMA

The same active substance is authorised in 2 EEA countries. Names it is sold under:

  • Germany · D-Fluoretten, Dekristol Fluor
  • Luxembourg · Fluor-Vigantol

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/c2840261-7f6c-40eb-b827-3c2fe381ae22
GET /v1/drugs/c2840261-7f6c-40eb-b827-3c2fe381ae22?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": "66498605",
  "date_amm": "2001-05-31",
  "type_amm": "Procédure nationale",
  "numero_ue": null,
  "substance": "FLUORURE DE SODIUM + CONCENTRAT DE CHOLÉCALCIFÉROL, FORME PULVÉRULENTE",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "solution buvable",
  "voies_administration": "orale",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Non"
}

See everything about fluorure de sodium + concentrat de cholécalciférol, forme pulvérulente.

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.