FDA — authorised 26 February 2004
- Application: BLA125085
- Marketing authorisation holder: GENENTECH
- Local brand name: AVASTIN
- Indication: VIAL — INTRAVENOUS
- Status: approved
FDA authorised carboplatin paclitaxel bevacizumab on 26 February 2004
Yes. FDA authorised it on 26 February 2004.
GENENTECH holds the US marketing authorisation.