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France· FR:69941714

DIOSMINE BIOGARAN CONSEIL 600 mg, comprimé pelliculé

A medicinal product containing diosmine, registered in France by BIOGARAN.

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…normalisedDIOSMINE BIOGARAN CONSEIL 600 mg, com…ATC—REGISTER NO.FR:69941714PACKS LISTED1CHECKEDSeptember 12, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about diosmineAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

The record

At a glance

Base de données publique des médicaments — BDPM (France)
Active substance
DIOSMINE
Manufacturer
BIOGARAN
Country
France (FR)
ATC code
—
Reimbursed
No
Source register
Base de données publique des médicaments — BDPM (France)
Last checked
September 12, 2026

Packs & prices · 1

  • cip13
    3400935618160
    plaquette(s) PVC-Aluminium de 30 comprimé(s)

Regulatory notes

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

Same medicine, other countries

Diosmine in 5 other countries

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

All diosmine products

Authorised across Europe · EMA

The same active substance is authorised in 18 EEA countries. Names it is sold under:

  • Austria · Diosmin Genericon, Diosmin Stada
  • Belgium · Diosmin Eg
  • Bulgaria · ??? ???? Film - Coated Tablets, Phlebodia
  • Czechia · Diosmin Stada, Diozen
  • Estonia · Flebaven, Viviton
  • Spain · Dioflav, Diosmina Cinfalab
  • Greece · Radiavit
  • Croatia · Diosmin Stada, Duodin
  • Hungary · Dio-Pp, Donimok
  • Italy · Alvenex, Diosven
  • Lithuania · Fladios, Legilait
  • Latvia · Flabien, Phlebodia
  • Malta · Dimotec, Phlebodia
  • Poland · Dih, Dih Max Comfort
  • Portugal · Diosmina Odel, Diosmina Venosmil
  • Romania · Flebazol, Hivis
  • Slovenia · Flebaven
  • Slovakia · Diosmin Stada, Diozen

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/e0401904-8337-4410-a556-ff2d7ef99fa8
GET /v1/drugs/e0401904-8337-4410-a556-ff2d7ef99fa8?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": "69941714",
  "date_amm": "2001-02-16",
  "type_amm": "Procédure nationale",
  "numero_ue": null,
  "substance": "DIOSMINE",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "comprimé pelliculé",
  "voies_administration": "orale",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Non"
}
API referenceMCP serverPlans

See everything about diosmine.

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.

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