FDA — authorised 20 July 2011
- Application: NDA022433
- Marketing authorisation holder: ASTRAZENECA
- Status: supplemented
FDA authorised Brilinta on 20 July 2011
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 20 July 2011; FDA has authorised it.
ASTRAZENECA holds the US marketing authorisation.