EMA — authorised 31 December 2009
- Application: EMEA/H/C/000747
- Marketing authorisation holder: Schering-Plough Europe
- Local brand name: Garenoxacin mesylate
- Status: withdrawn
EMA authorised GARENOXACIN MESYLATE on 31 December 2009
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. EMA authorised it on 31 December 2009.
Schering-Plough Europe holds the EU marketing authorisation.