FDA — authorised 5 December 2008
- Application: NDA022214
- Marketing authorisation holder: ASTRAZENECA
- Local brand name: ARIMIDEX
- Indication: TABLET — ORAL
- Status: approved
FDA authorised Anastrazole (Arimidex) on 5 December 2008
Yes. FDA authorised it on 5 December 2008.
ASTRAZENECA holds the US marketing authorisation.