FDA — authorised 20 December 2024
- Application: NDA218730
- Marketing authorisation holder: VERTEX PHARMS INC
- Local brand name: ALYFTREK
- Indication: TABLET — ORAL
- Status: approved
FDA authorised Alyftrek on 20 December 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 December 2024; FDA has authorised it.
VERTEX PHARMS INC holds the US marketing authorisation.