Nonafact (human coagulation factor IX)
- Region
- 🇪🇺 EU
- Active substance
- human coagulation factor IX
- Company
- Sanquin Plasma Products B.V.
- Status
- Withdrawn
- Therapeutic area
- Hemophilia B
- EU approval
- Tue 03 Jul 2001
- Application
- EMEA/H/C/000348
- ATC
- B02BD04
- Official record
- www.ema.europa.eu
Indication
Treatment and prophylaxis of bleeding in patients with haemophilia B (congenital factor IX deficiency).
Regulatory milestones
No milestones recorded in the last year.
Follow Nonafact
Get VigiEye Daily: approvals, opinions, safety actions and PDUFA dates every morning.
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.