France· FR:69594306
CELLCEPT 1 g/5 mL, poudre pour suspension buvable
A medicinal product containing mycophénolate mofétil, registered in France by ROCHE REGISTRATION (ALLEMAGNE), 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
- MYCOPHÉNOLATE MOFÉTIL
- Manufacturer
- ROCHE REGISTRATION (ALLEMAGNE)
- Country
- France (FR)
- ATC code
- —
- Reimbursed
- Yes
- Source register
- Base de données publique des médicaments — BDPM (France)
- Last checked
- September 12, 2026
Packs & prices · 4
4 priced- cip1334009359529361 flacon(s) polyéthylène haute densité (PEHD) avec seringue(s) pour administration orale de 110 gEUR 186.77
- cip1334009495011131 flacon(s) polyéthylène haute densité (PEHD) avec seringue(s) pour administration orale de 110 g (distributeur parallèle : BB Farma)EUR 177.49
- cip1334009495012051 flacon(s) polyéthylène haute densité (PEHD) avec seringue(s) pour administration orale de 110 g (distributeur parallèle : Abacus Medicine A/S).EUR 177.49
- cip1334009495015401 flacon polyéthylène haute densité (PEHD) avec seringue pour administration orale de 110 g (distributeur parallèle : Difarmed)EUR 177.49
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Mycophénolate mofétil in 10 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesCellCeptGenentech, Inc.
- FinlandCellceptAbacus Medicine A/S
- BelgiumCellcept 1 g/5 mlRoche Registration
- NorwayCellCeptRoche Registration GmbH
- SwedenCellCept 1 g/5 ml Pulver till oral suspensionRoche Registration GmbH
- IrelandCellCept 1 g/5 ml Powder for oral suspensionRoche Registration GmbH
- CzechiaCELLCEPTRoche Registration GmbH, Grenzach-Wyhlen
- United KingdomArzip 250mg capsulesZentiva Pharma UK Ltd
Authorised across Europe · EMA
The same active substance is authorised in 25 EEA countries. Names it is sold under:
- Austria · Mowel, Mycophenolat Mofetil Sandoz
- Belgium · Mycophenolat Mofetil Sandoz
- Bulgaria · Микофенолат Мофетил Акорд
- Czechia · Mycophenolat Mofetil Sandoz
- Germany · Mowel, Mycophenolat 1 A Pharma
- Denmark · Mycophenolate Mofetil Hexal, Mycophenolatmofetil Accord
- Estonia · Mycophenolate Mofetil Accord
- Spain · Micofenolato De Mofetilo Accord, Micofenolato De Mofetilo Aristo
- Finland · Mycophenolate Mofetil Accord, Mycophenolate Mofetil Eql Pharma
- United Kingdom (Northern Ireland) · Mycophenolate Hexal, Mycophenolate Mofetil
- Croatia · Mofetilmikofenolat Tillomed, Trixin
- Ireland · Mycolat, Mycophenolate Mofetil Accord
- Iceland · Cellcept, Myclausen
- Italy · Micofenolato Mofetile Accord, Micofenolato Mofetile Ahcl
- Liechtenstein · Cellcept, Myclausen
- Lithuania · Mycophenolate Mofetil Accord
- Latvia · Mycophenolate Mofetil Accord
- Malta · Mycophenolate Mofetil Ascend
- Netherlands · Mycofenolaat Mofetil Accord, Mycofenolaat Mofetil Sandoz
- Norway · Cellcept, Myclausen
- Poland · Mycofit, Mycophenolate Mofetil Sandoz
- Portugal · Micofenolato De Mofetil Accord, Micofenolato De Mofetil Aristo
- Romania · Micofenolat Mofetil Sandoz
- Sweden · Mycophenolate Mofetil Accord, Mycophenolate Mofetil Eql Pharma
- Slovakia · Mykofenolát Mofetil Sandoz
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/2c1be6e9-7f19-4144-adcc-00081297f08d GET /v1/drugs/2c1be6e9-7f19-4144-adcc-00081297f08d?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": "69594306",
"date_amm": "1999-02-26",
"type_amm": "Procédure centralisée",
"numero_ue": "EU/1/96/005",
"substance": "MYCOPHÉNOLATE MOFÉTIL",
"statut_amm": "Autorisation active",
"statut_bdm": null,
"forme_pharmaceutique": "poudre pour suspension buvable",
"voies_administration": "orale",
"etat_commercialisation": "Commercialisée",
"surveillance_renforcee": "Non"
}See everything about mycophénolate mofétil.
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.