🇺🇸 Apixaban Oral Tablet [Eliquis] in United States

FDA authorised Apixaban Oral Tablet [Eliquis] on 28 December 2012

Marketing authorisations

FDA — authorised 28 December 2012

  • Application: NDA202155
  • Marketing authorisation holder: BRISTOL MYERS SQUIBB
  • Local brand name: ELIQUIS
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 17 April 2025

  • Application: NDA220073
  • Marketing authorisation holder: BRISTOL
  • Local brand name: ELIQUIS
  • Indication: TABLET — ORAL
  • Status: approved

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Frequently asked questions

Is Apixaban Oral Tablet [Eliquis] approved in United States?

Yes. FDA authorised it on 28 December 2012; FDA authorised it on 17 April 2025.

Who is the marketing authorisation holder for Apixaban Oral Tablet [Eliquis] in United States?

BRISTOL MYERS SQUIBB holds the US marketing authorisation.