FDA — authorised 27 September 2022
- Application: BLA761268
- Marketing authorisation holder: CELLTRION
- Local brand name: VEGZELMA
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised VEGZELMA on 27 September 2022
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 27 September 2022; FDA has authorised it.
CELLTRION holds the US marketing authorisation.