FDA — authorised 20 March 2018
- Application: BLA761067
- Marketing authorisation holder: SUN PHARMA GLOBAL
- Local brand name: ILUMYA
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised ILUMYA on 20 March 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 20 March 2018.
SUN PHARMA GLOBAL holds the US marketing authorisation.