🇪🇺 TAK-491 in European Union

EMA authorised TAK-491 on 7 December 2011

Marketing authorisations

EMA — authorised 7 December 2011

  • Application: EMEA/H/C/002293
  • Marketing authorisation holder: Takeda Pharma A/S
  • Local brand name: Edarbi
  • Indication: Edarbi is indicated for the treatment of essential hypertension in adults.
  • Status: approved

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EMA — authorised 7 December 2011

  • Application: EMEA/H/C/002517
  • Marketing authorisation holder: Takeda Pharma A/S
  • Local brand name: Ipreziv
  • Indication: Ipreziv is indicated for the treatment of essential hypertension in adults.
  • Status: withdrawn

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Frequently asked questions

Is TAK-491 approved in European Union?

Yes. EMA authorised it on 7 December 2011; EMA authorised it on 7 December 2011.

Who is the marketing authorisation holder for TAK-491 in European Union?

Takeda Pharma A/S holds the EU marketing authorisation.