Advagraf (tacrolimus)
- Region
- 🇪🇺 EU
- Active substance
- tacrolimus
- Company
- Astellas Pharma Europe BV
- Status
- Authorised
- Therapeutic area
- Graft Rejection
- EU approval
- Mon 23 Apr 2007
- Application
- EMEA/H/C/000712
- ATC
- L04AD02
- Official record
- www.ema.europa.eu
Indication
Prophylaxis of transplant rejection in adult kidney or liver allograft recipients. Treatment of allograft rejection resistant to treatment with other immunosuppressive medicinal products in adult patients.
Regulatory milestones
No milestones recorded in the last year.
Same substance in other markets
- 🇪🇺 Protopic Authorised · LEO Pharma A/S
- 🇪🇺 Tacforius Authorised · Teva B.V.
- 🇪🇺 Envarsus Authorised · Chiesi Farmaceutici S.p.A.
- 🇪🇺 Modigraf Authorised · Astellas Pharma Europe B.V.
- 🇪🇺 Protopy Withdrawn · Astellas Pharma GmbH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.