EMA — authorised 23 November 2011
- Application: EMEA/H/C/002200
- Marketing authorisation holder: Dyax s.a.
- Local brand name: Kalbitor
- Status: withdrawn
EMA authorised Kalbitor on 23 November 2011
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. EMA authorised it on 23 November 2011.
Dyax s.a. holds the EU marketing authorisation.