France· FR:67148682
OSAFLEXAN 1178 mg, poudre pour solution buvable en sachet-dose
A glucosamine product containing sulfate de glucosamine, registered in France by COOPER CONSUMER NETHERLANDS (PAYS-BAS). The same ATC class is registered in 14 of our 19 countries.
Checked against Base de données publique des médicaments — BDPM (France) on
Informational only — not a medical device.
Where it is registered
Glucosamine is registered in 14 of 19 countries.
Countries holding a registration under ATC M01AX05 (glucosamine), each read from that country’s own register.
- This record: France, from Base de données publique des médicaments — BDPM (France)
- 8 of them publish a price we can compare per daily dose
Glucosamine · ATC M01AX05
14 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Germany
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Spainprice
- Sweden
- United Kingdom
Price per daily dose
What a daily dose of glucosamine costs, country by country.
Normalised to the WHO defined daily dose (1.5 g), so markets compare like for like.
- 1 market with a comparable price for this class
- Public list prices, converted to USD at the rate date shown
Glucosamine · price per daily dose (1.5 g)
USD · FX 28 Sept 2026
- ES Spain$0.23
The record
At a glance
Base de données publique des médicaments — BDPM (France)- Active substance
- SULFATE DE GLUCOSAMINE
- Manufacturer
- COOPER CONSUMER NETHERLANDS (PAYS-BAS)
- Country
- France (FR)
- ATC code
- M01AX05
- ATC class
- Glucosamine
- Defined daily dose
- 1.5 g, O
- Reimbursed
- No
- Source register
- Base de données publique des médicaments — BDPM (France)
- Last checked
- September 12, 2026
Packs & prices · 1
- cip13340093970182030 sachet(s)-dose(s) papier aluminium polyéthylène
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
2 interactions on record for glucosamine.
Graded by severity as the source publishes them — 2 moderate. Severity grades are free for everyone; mechanism and management come with Growth.
- Severity for every pair — free, no plan needed
- The source, licence and sync date on every record
- Mechanism and what to do for each pair — Growth plan
Glucosamine · interactions on record
2 records
- 2 moderate
Most severe, free to view
- DicoumarolB01AA01moderate
- WarfarinB01AA03moderate
- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Same medicine, other countries
Glucosamine in 11 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomAlateris 625mg tabletsMWK Healthcare Ltd
- PolandArthrylDelfarma Sp. z o.o.
- CzechiaARTAXINLaboratorio Reig Jofré S.A., Barcelona
- SpainACENAM 1250 mg COMPRIMIDOS EFERVESCENTESEspecialidades Farmaceuticas Centrum S.A.
- SwedenArtroxan 625 mg Kapsel, hårdEvolan Pharma AB
- IrelandArthrimel 1500mg Film Coated TabletsPhoenix Labs
- FinlandGiscosamineE-Pharma Trento S.p.A.
- NetherlandsDolenio 1178 mg, filmomhulde tabletBlue Bio Pharmaceuticals Limited
Authorised across Europe · EMA
The same active substance is authorised in 15 EEA countries. Names it is sold under:
- Cyprus · Donarthril
- Czechia · Artaxin, Flexove
- Germany · Glucosamin Doppelherzpharma
- Spain · Acenam, Duartron
- Finland · Glucosamin Orion
- United Kingdom (Northern Ireland) · Glucosamine Medley Pharma, Yointy
- Greece · Donarot, Energorot
- Hungary · Cartilamin, Glukozamin Pharma Nord
- Ireland · Arthrimel, Dona
- Iceland · Glucomed
- Norway · Glucosamin Orifarm, Samin
- Poland · Flexove
- Portugal · Biartril, Glucomed
- Sweden · Artroxan, Glucomed
- Slovakia · Glucomed
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/07dde0b3-bd15-4382-b9b2-923dbcc98f10 GET /v1/drugs/07dde0b3-bd15-4382-b9b2-923dbcc98f10?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": "67148682",
"date_amm": "2009-10-06",
"type_amm": "Procédure décentralisée",
"numero_ue": null,
"substance": "SULFATE DE GLUCOSAMINE",
"atc_source": "fr_atc_restore_2026-09-06",
"statut_amm": "Autorisation active",
"statut_bdm": null,
"forme_pharmaceutique": "poudre pour solution buvable",
"voies_administration": "orale",
"etat_commercialisation": "Commercialisée",
"surveillance_renforcee": "Non"
}See everything about glucosamine.
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.