France· FR:61444482
DIVINA, comprimé
A medicinal product containing valérate d'estradiol + acétate de médroxyprogestérone, registered in France by ORION CORPORATION, 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
- VALÉRATE D'ESTRADIOL + ACÉTATE DE MÉDROXYPROGESTÉRONE
- Manufacturer
- ORION CORPORATION
- 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- cip1334009334435591 plaquette(s) PVC-Aluminium PVDC de 10 comprimé(s) - 1 plaquette(s) de 11 comprimé(s)EUR 6.25
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Valérate d'estradiol + acétate de médroxyprogestérone in 8 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomEstradiol valerate 2mg / Medroxyprogesterone 20mg tabletsWaymade Healthcare Plc
- FinlandDivinaOrion Corporation
- CzechiaINDIVINAOrion Corporation, Espoo
- NorwayIndivinaOrion Corporation
- SwedenIndivina 1 mg/2,5 mg TablettOrion Corporation
- SwitzerlandIndivina
- GermanyIndivinaOrion Corporation
- SpainPERIFEM 2 mg/10 mg COMPRIMIDOSOrion Corporation
Authorised across Europe · EMA
The same active substance is authorised in 7 EEA countries. Names it is sold under:
- Czechia · Indivina
- Germany · Indivina
- Denmark · Indivina
- Finland · Indivina
- United Kingdom (Northern Ireland) · Indivina
- Norway · Indivina
- Sweden · Indivina
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/53e28aaa-e60f-45a2-8ea8-ef4e5ab4c1eb GET /v1/drugs/53e28aaa-e60f-45a2-8ea8-ef4e5ab4c1eb?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": "61444482",
"date_amm": "1991-12-02",
"type_amm": "Procédure nationale",
"numero_ue": null,
"substance": "VALÉRATE D'ESTRADIOL + ACÉTATE DE MÉDROXYPROGESTÉRONE",
"statut_amm": "Autorisation abrogée",
"statut_bdm": "Warning disponibilité",
"forme_pharmaceutique": "comprimé et comprimé",
"voies_administration": "orale",
"etat_commercialisation": "Non commercialisée",
"surveillance_renforcee": "Non"
}See everything about valérate d'estradiol + acétate de médroxyprogestérone.
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.