🇪🇺 GARENOXACIN MESYLATE in European Union

EMA authorised GARENOXACIN MESYLATE on 31 December 2009

Marketing authorisation

EMA — authorised 31 December 2009

  • Application: EMEA/H/C/000747
  • Marketing authorisation holder: Schering-Plough Europe
  • Local brand name: Garenoxacin mesylate
  • Status: withdrawn

Read official source →

GARENOXACIN MESYLATE in other countries

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

Frequently asked questions

Is GARENOXACIN MESYLATE approved in European Union?

Yes. EMA authorised it on 31 December 2009.

Who is the marketing authorisation holder for GARENOXACIN MESYLATE in European Union?

Schering-Plough Europe holds the EU marketing authorisation.