FDA — authorised 30 June 2006
- Application: BLA125156
- Marketing authorisation holder: GENENTECH
- Status: supplemented
FDA authorised Lucentis on 30 June 2006
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 30 June 2006; FDA has authorised it.
GENENTECH holds the US marketing authorisation.