🇪🇺 Daklinza in European Union

EMA authorised Daklinza on 27 June 2014

Marketing authorisation

EMA — authorised 27 June 2014

  • Status: approved

Daklinza in other countries

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

Other Oncology approved in European Union

Frequently asked questions

Is Daklinza approved in European Union?

Yes. EMA authorised it on 27 June 2014.

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

Bristol-Myers Squibb is the originator. The local marketing authorisation holder may differ — check the official source linked above.