FDA — authorised 13 December 2017
- Application: BLA761072
- Marketing authorisation holder: PFIZER INC
- Local brand name: IXIFI
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised IXIFI on 13 December 2017
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 13 December 2017; FDA has authorised it.
PFIZER INC holds the US marketing authorisation.