FDA — authorised 25 July 1997
- Application: NDA020726
- Marketing authorisation holder: NOVARTIS PHARMS
- Local brand name: FEMARA
- Indication: TABLET — ORAL
- Status: approved
FDA authorised Femara on 25 July 1997
Yes. FDA authorised it on 25 July 1997.
NOVARTIS PHARMS holds the US marketing authorisation.