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France· FR:62296848

RHEOFLUX 3500 mg, poudre pour solution buvable en sachet-dose

A medicinal product containing troxérutine, registered in France by ETHYX PHARMACEUTICALS.

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…normalisedRHEOFLUX 3500 mg, poudre pour solutio…ATC—REGISTER NO.FR:62296848PACKS LISTED1CHECKEDSeptember 12, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about troxérutineAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

The record

At a glance

Base de données publique des médicaments — BDPM (France)
Active substance
TROXÉRUTINE
Manufacturer
ETHYX PHARMACEUTICALS
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
    3400933627843
    10 sachet(s) papier aluminium polyéthylène de 7,25 g

Regulatory notes

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

Same medicine, other countries

Troxérutine in 5 other countries

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

All troxérutine products

Authorised across Europe · EMA

The same active substance is authorised in 20 EEA countries. Names it is sold under:

  • Austria · Venoruton, Venoruton - Gel
  • Belgium · Venoruton, Venoruton Beutel
  • Bulgaria · Троксевазин, Троксерутин Абр
  • Czechia · Cilkanol, Venoruton
  • Germany · Veno Sl 300, Veno-Pos
  • Denmark · Venoruton
  • Estonia · Troxevasin, Troxevasin Teva
  • Spain · Esberiven, Troxerutina Cinfalab
  • United Kingdom (Northern Ireland) · Paroven
  • Greece · Venoruton
  • Hungary · Venoruton
  • Italy · Venolen, Venoruton
  • Lithuania · Troxevasin, Venoruton
  • Luxembourg · O-(B-Hydroxyaethyl)-Rutosidea Eg (Eurogenerics) Sa, O-(B-Hydroxyethyl)-Rutosidea Eg (Eurogenerics) Sa
  • Latvia · Troxerutin Sopharma, Troxevasin
  • Netherlands · Venoruton
  • Poland · Posorutin, Rutoven
  • Portugal · Venoruton
  • Romania · Devaricid Gel, Troxerutin Chirmis
  • Slovakia · Cilkanol, Venoruton

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/f4ec4645-5b45-4313-8a6b-78089632a6bc
GET /v1/drugs/f4ec4645-5b45-4313-8a6b-78089632a6bc?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": "62296848",
  "date_amm": "1993-08-03",
  "type_amm": "Procédure nationale",
  "numero_ue": null,
  "substance": "TROXÉRUTINE",
  "statut_amm": "Autorisation active",
  "statut_bdm": "Warning disponibilité",
  "forme_pharmaceutique": "poudre pour solution buvable",
  "voies_administration": "orale",
  "etat_commercialisation": "Non commercialisée",
  "surveillance_renforcee": "Non"
}
API referenceMCP serverPlans

See everything about troxérutine.

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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