Mycophenolate mofetil Teva (mycophenolate mofetil)
Generic
- Region
- 🇪🇺 EU
- Active substance
- mycophenolate mofetil
- Company
- Teva Pharma B.V.
- Status
- Authorised
- Therapeutic area
- Graft Rejection
- CHMP opinion
- Thu 13 Dec 2007
- EU approval
- Thu 21 Feb 2008
- Designations
- Generic
- Application
- EMEA/H/C/000882
- ATC
- L04AA06
- Official record
- www.ema.europa.eu
Indication
Mycophenolate mofetil Teva is indicated in combination with ciclosporin and corticosteroids for the prophylaxis of acute transplant rejection in patients receiving allogeneic renal, cardiac or hepatic transplants.
Regulatory milestones
No milestones recorded in the last year.
Same substance in other markets
- 🇪🇺 CellCept Authorised · Roche Registration GmbH
- 🇪🇺 Myfenax Authorised · Teva B.V.
- 🇪🇺 Myclausen Authorised · Passauer Pharma GmbH
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Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.