🇪🇺 Anxa in European Union

EMA authorised Anxa on 26 April 2019

Marketing authorisation

EMA — authorised 26 April 2019

  • Marketing authorisation holder: Portola Netherlands BV
  • Status: approved

Anxa 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 European Union

Frequently asked questions

Is Anxa approved in European Union?

Yes. EMA authorised it on 26 April 2019.

Who is the marketing authorisation holder for Anxa in European Union?

Portola Netherlands BV holds the EU marketing authorisation.