FDA — authorised 13 March 2024
- Application: BLA761232
- Marketing authorisation holder: BEIGENE
- Local brand name: TEVIMBRA
- Indication: INJECTION — SOLUTION
- Status: approved
FDA authorised TEVIMBRA on 13 March 2024
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 13 March 2024; FDA has authorised it.
BEIGENE holds the US marketing authorisation.