FDA — authorised 25 September 2025
- Application: NDA218881
- Marketing authorisation holder: ELI LILLY AND CO
- Local brand name: INLURIYO
- Indication: TABLET — ORAL
- Status: approved
FDA authorised Inluriyo on 25 September 2025
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 25 September 2025; FDA has authorised it.
ELI LILLY AND CO holds the US marketing authorisation.