Irbesartan BMS

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Withdrawn

This medicine's authorisation has been withdrawn

irbesartan
MedicineHumanWithdrawn

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  • Application under evaluation
  • CHMP opinion
  • European Commission decision

Overview

Introduction

On 19 January 2007 the European Commission issued a Marketing Authorisation valid throughout the European Union for the medicinal product Irbesartan BMS (irbesartan). Irbesartan BMS is approved for the treatment of essential hypertension and the treatment of renal disease in patients with hypertension and type 2 diabetes mellitus as part of an antihypertensive medicinal product regimen. The marketing authorisation holder (MAH) responsible for Irbesartan BMS was Bristol-Myers Squibb Pharma EEIG. 

The European Commission was notified by letter dated 20 October 2009 of the MAH’s decision to voluntarily withdraw the Marketing Authorisation for Irbesartan BMS for commercial reasons. Irbesartan BMS has not been marketed anywhere in the European Union and there is no intention to market Irbesartan BMS in the future. Irbesartan BMS was an informed consent application to Karvea. The MAH will maintain the Marketing Authorisation for another medicinal product containing irbesartan, i.e. Karvea. 

On 11 November 2009 the European Commission issued a decision to withdraw the marketing authorisation for Irbesartan BMS. 

Pursuant to this decision the European Public Assessment Report for Irbesartan BMS is updated to reflect that the Marketing Authorisation is no longer valid.

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Product information

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Latest procedure affecting product information:II/0018
07/04/2009
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This medicine’s product information is available in all official EU languages.
Select 'available languages' to access the language you need.

 

Product information documents contain:

  • summary of product characteristics (annex I);
  • manufacturing authorisation holder responsible for batch release (annex IIA);
  • conditions of the marketing authorisation (annex IIB);
  • labelling (annex IIIA);
  • package leaflet (annex IIIB).

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Product details

Name of medicine
Irbesartan BMS
Active substance
irbesartan
International non-proprietary name (INN) or common name
irbesartan
Therapeutic area (MeSH)
Hypertension
Anatomical therapeutic chemical (ATC) code
C09CA04

Pharmacotherapeutic group

Agents acting on the renin-angiotensin system

Therapeutic indication

Treatment of essential hypertension.
Treatment of renal disease in patients with hypertension and type 2 diabetes mellitus as part of an antihypertensive medicinal product regimen (see section 5.1).

Authorisation details

EMA product number
EMEA/H/C/000786
Marketing authorisation holder
Bristol-Myers Squibb Pharma EEIG

Plaza 254
Blanchardstown Corporate Park 2
Dublin 15, D15 T867
Ireland

Marketing authorisation issued
19/01/2007
Withdrawal of marketing authorisation
11/11/2009
Revision
7

Assessment history

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