FDA — authorised 7 October 2019
- Application: BLA761125
- Marketing authorisation holder: NOVARTIS PHARMS CORP
- Local brand name: BEOVU
- Indication: INJECTABLE — INTRAVITREAL
- Status: approved
FDA authorised Beovu on 7 October 2019
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 7 October 2019.
NOVARTIS PHARMS CORP holds the US marketing authorisation.