FDA — authorised 9 August 2024
- Application: BLA761382
- Marketing authorisation holder: SANDOZ INC
- Local brand name: ENZEEVU
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised ENZEEVU on 9 August 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 9 August 2024; FDA has authorised it.
SANDOZ INC holds the US marketing authorisation.