FDA — authorised 17 June 2009
- Application: BLA125319
- Marketing authorisation holder: NOVARTIS PHARMS
- Local brand name: ILARIS
- Indication: INJECTABLE — SUBCUTANEOUS
- Status: approved
FDA authorised Ilaris on 17 June 2009
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 17 June 2009.
NOVARTIS PHARMS holds the US marketing authorisation.