🇺🇸 Pradaxa in United States

FDA authorised Pradaxa on 19 October 2010

Marketing authorisations

FDA — authorised 19 October 2010

  • Marketing authorisation holder: BOEHRINGER INGELHEIM
  • Status: approved

FDA — authorised 15 December 2023

  • Application: ANDA208070
  • Marketing authorisation holder: APOTEX
  • Status: approved

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FDA — authorised 11 September 2024

  • Application: ANDA208040
  • Marketing authorisation holder: ALKEM LABS LTD
  • Status: approved

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FDA — authorised 28 January 2025

  • Application: ANDA208048
  • Marketing authorisation holder: DR REDDYS
  • Status: approved

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FDA — authorised 3 February 2025

  • Application: ANDA208067
  • Marketing authorisation holder: MYLAN
  • Status: approved

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FDA — authorised 14 May 2025

  • Application: ANDA208039
  • Marketing authorisation holder: AUROBINDO PHARMA
  • Status: approved

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Pradaxa in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Other Cardiovascular approved in United States

Frequently asked questions

Is Pradaxa approved in United States?

Yes. FDA authorised it on 19 October 2010; FDA authorised it on 15 December 2023; FDA authorised it on 11 September 2024.

Who is the marketing authorisation holder for Pradaxa in United States?

BOEHRINGER INGELHEIM holds the US marketing authorisation.