🇪🇺 Aimovig in European Union

EMA authorised Aimovig on 26 July 2018

Marketing authorisation

EMA — authorised 26 July 2018

  • Marketing authorisation holder: NOVARTIS EUROPHARM LIMITED
  • Status: approved

Aimovig in other countries

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

Other Neuroscience approved in European Union

Frequently asked questions

Is Aimovig approved in European Union?

Yes. EMA authorised it on 26 July 2018.

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

NOVARTIS EUROPHARM LIMITED holds the EU marketing authorisation.