FDA — authorised 10 August 2018
- Application: NDA210922
- Marketing authorisation holder: ALNYLAM PHARMS INC
- Local brand name: ONPATTRO
- Indication: SOLUTION — INTRAVENOUS
- Status: approved
FDA authorised Onpattro on 10 August 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 10 August 2018; FDA has authorised it.
ALNYLAM PHARMS INC holds the US marketing authorisation.