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France· FR:65084900

STRUCTUM 500 mg, gélule

A medicinal product containing chondroïtine (sulfate de) sodique, registered in France by PIERRE FABRE MEDICAMENT.

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…normalisedSTRUCTUM 500 mg, géluleATC—REGISTER NO.FR:65084900PACKS LISTED1CHECKEDSeptember 12, 2026

The record

At a glance

Base de données publique des médicaments — BDPM (France)
Active substance
CHONDROÏTINE (SULFATE DE) SODIQUE
Manufacturer
PIERRE FABRE MEDICAMENT
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
    3400935464323
    plaquette(s) thermoformée(s) PVC PVDC aluminium-laque de 60 gélule(s)

Regulatory notes

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

Same medicine, other countries

Chondroïtine (sulfate de) sodique in 10 other countries

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

All chondroïtine (sulfate de) sodique products

Authorised across Europe · EMA

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

  • Austria · Cartexan, Condrosulf
  • Belgium · Hirudoid
  • Czechia · Condrodin, Condrosulf
  • Germany · Hirudoid, Hirudoid Forte
  • Denmark · Hirudoid
  • Spain · Condrodin, Condroitín Sulfato Kern Pharma
  • Finland · Cartexan, Cartexan Laboratorio Reig Jofre, S.A.
  • United Kingdom (Northern Ireland) · Hirudoid, Hirudoid Gel
  • Greece · Condromed
  • Hungary · Cartexan, Condrosulf
  • Iceland · Hirudoid
  • Italy · Condral, Condrosulf
  • Luxembourg · Hirudoid
  • Netherlands · Hirudoid
  • Norway · Hirudoid
  • Poland · Cartexan, Condromed
  • Portugal · Hirudoid, Ossin
  • Romania · Hirudoid
  • Sweden · Hirudoid
  • Slovakia · Condrosulf, Hirudoid Forte

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/f966bcc2-fb5a-43b2-9290-d6c5d15a3cfb
GET /v1/drugs/f966bcc2-fb5a-43b2-9290-d6c5d15a3cfb?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": "65084900",
  "date_amm": "2001-01-04",
  "type_amm": "Procédure nationale",
  "numero_ue": null,
  "substance": "CHONDROÏTINE (SULFATE DE) SODIQUE",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "gélule",
  "voies_administration": "orale",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Non"
}

See everything about chondroïtine (sulfate de) sodique.

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.