FDA — authorised 2 October 2017
- Application: NDA208772
- Marketing authorisation holder: TAKEDA PHARMS USA
- Indication: Manufacturing (CMC)
- Status: approved
FDA authorised Alunbrig on 2 October 2017
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 2 October 2017.
TAKEDA PHARMS USA holds the US marketing authorisation.