FDA — authorised 28 December 2012
- Application: NDA202155
- Marketing authorisation holder: BRISTOL MYERS SQUIBB
- Local brand name: ELIQUIS
- Indication: TABLET — ORAL
- Status: approved
FDA authorised Apixaban Oral Tablet [Eliquis] on 28 December 2012
Yes. FDA authorised it on 28 December 2012; FDA authorised it on 17 April 2025.
BRISTOL MYERS SQUIBB holds the US marketing authorisation.