FDA — authorised 7 June 2000
- Application: BLA020986
- Marketing authorisation holder: NOVO NORDISK INC
- Status: supplemented
FDA authorised Aspart on 7 June 2000
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 7 June 2000; FDA authorised it on 1 November 2001; FDA has authorised it.
NOVO NORDISK INC holds the US marketing authorisation.