FDA — authorised 8 January 2015
- Application: NDA206316
- Marketing authorisation holder: DAIICHI SANKYO INC
- Local brand name: SAVAYSA
- Indication: TABLET — ORAL
- Status: approved
FDA authorised Savaysa on 8 January 2015
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 8 January 2015.
DAIICHI SANKYO INC holds the US marketing authorisation.