FDA — authorised 10 October 1989
- Application: NDA019687
- Marketing authorisation holder: FERRING
- Local brand name: LUTREPULSE KIT
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised GONADORELIN ACETATE on 10 October 1989
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 10 October 1989; FDA has authorised it.
FERRING holds the US marketing authorisation.