FDA — authorised 20 June 2000
- Application: BLA021148
- Marketing authorisation holder: NOVO NORDISK INC
- Local brand name: NORDITROPIN NORDIFLEX
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised Norditropin NordiFlex® on 20 June 2000
Yes. FDA authorised it on 20 June 2000.
NOVO NORDISK INC holds the US marketing authorisation.