FDA — authorised 31 May 2018
- Application: NDA207924
- Marketing authorisation holder: ELI LILLY AND CO
- Indication: Type 1 - New Molecular Entity
- Status: approved
FDA authorised Olumiant on 31 May 2018
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 31 May 2018.
ELI LILLY AND CO holds the US marketing authorisation.