🇪🇺 Banzel in European Union

EMA authorised Banzel on 16 January 2007

Marketing authorisations

EMA — authorised 16 January 2007

  • Marketing authorisation holder: Eisai Ltd
  • Status: approved

EMA — authorised 16 January 2007

  • Application: EMEA/H/C/000660
  • Marketing authorisation holder: Eisai GmbH
  • Local brand name: Inovelon
  • Indication: Inovelon is indicated as adjunctive therapy in the treatment of seizures associated with Lennox Gastaut syndrome in patients 4 years of age and older.
  • Status: approved

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Banzel 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 Banzel approved in European Union?

Yes. EMA authorised it on 16 January 2007; EMA authorised it on 16 January 2007.

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

Eisai Ltd holds the EU marketing authorisation.