FDA — authorised 14 August 1987
- Application: NDA019763
- Marketing authorisation holder: BAXTER HLTHCARE
- Local brand name: IFEX
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised Ifex on 14 August 1987
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 14 August 1987; FDA authorised it on 30 December 1988.
BAXTER HLTHCARE holds the US marketing authorisation.