France· FR:61878240
RISEDRONATE VIATRIS 35 mg, comprimé pelliculé
A medicinal product containing risédronate monosodique hémipentahydraté, registered in France by VIATRIS SANTE, on the national reimbursement list.
Checked against Base de données publique des médicaments — BDPM (France) on
Informational only — not a medical device.
The record
At a glance
Base de données publique des médicaments — BDPM (France)- Active substance
- RISÉDRONATE MONOSODIQUE HÉMIPENTAHYDRATÉ
- Manufacturer
- VIATRIS SANTE
- Country
- France (FR)
- ATC code
- —
- Reimbursed
- Yes
- Source register
- Base de données publique des médicaments — BDPM (France)
- Last checked
- September 12, 2026
Packs & prices · 2
2 priced- cip133400949746156plaquette(s) thermoformée(s) de 4 comprimé(s)EUR 9.22
- cip133400949746385plaquette(s) thermoformée(s) de 12 comprimé(s)EUR 27.32
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Risédronate monosodique hémipentahydraté in 11 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SpainACREL SEMANAL 35 mg COMPRIMIDOS RECUBIERTOS CON PELICULATheramex Ireland Limited
- ItalyACTONELFARMED S.R.L.
- BelgiumActonel 35 mg HebdomadaireImpexeco
- NetherlandsNatriumrisedronaat Sandoz Wekelijks 35 mg, filmomhulde tablettenSandoz B.V.
- FinlandRisedronat PfizerPfizer Oy
- SwedenRisedronat Ebb 35 mg Filmdragerad tablettEbb Medical AB
- PolandRisendros 35Zentiva, k.s.
- IcelandRisedronate BluefishBluefish Pharmaceuticals AB
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- Germany · Risedronat Al
- Italy · Risedronato Eg Stada
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/02ecfed7-3682-4aa4-9377-0160d990f5fb GET /v1/drugs/02ecfed7-3682-4aa4-9377-0160d990f5fb?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": "61878240",
"date_amm": "2010-11-22",
"type_amm": "Procédure nationale",
"numero_ue": null,
"substance": "RISÉDRONATE MONOSODIQUE HÉMIPENTAHYDRATÉ",
"statut_amm": "Autorisation active",
"statut_bdm": null,
"forme_pharmaceutique": "comprimé pelliculé",
"voies_administration": "orale",
"etat_commercialisation": "Commercialisée",
"surveillance_renforcee": "Non"
}See everything about risédronate monosodique hémipentahydraté.
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.