FDA — authorised 20 May 2024
- Application: BLA761274
- Marketing authorisation holder: BIOCON BIOLOGICS INC
- Local brand name: YESAFILI
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised YESAFILI on 20 May 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 20 May 2024; FDA has authorised it.
BIOCON BIOLOGICS INC holds the US marketing authorisation.