🇪🇺 Kalbitor in European Union

EMA authorised Kalbitor on 23 November 2011

Marketing authorisation

EMA — authorised 23 November 2011

  • Application: EMEA/H/C/002200
  • Marketing authorisation holder: Dyax s.a.
  • Local brand name: Kalbitor
  • Status: withdrawn

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Kalbitor 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 Kalbitor approved in European Union?

Yes. EMA authorised it on 23 November 2011.

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

Dyax s.a. holds the EU marketing authorisation.