Enurev Breezhaler

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Withdrawn

This medicine's authorisation has been withdrawn

glycopyrronium bromide
MedicineHumanWithdrawn

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  • Application under evaluation
  • CHMP opinion
  • European Commission decision

Overview

On 30 August 2026, the European Commission withdrew the marketing authorisation for Enurev Breezhaler (Glycopyrronium bromide) in the European Union (EU). The withdrawal was at the request of the marketing authorisation holder, Novartis Europharm Limited, which notified the European Commission of its decision to permanently discontinue the marketing of the product for commercial reasons. 

Enurev Breezhaler was granted marketing authorisation in the EU on 28 September 2012 as maintenance bronchodilator treatment to relieve symptoms in adult patients with chronic obstructive pulmonary disease (COPD). 

The withdrawal of Enurev Breezhaler is not expected to have any impact on patient access
to treatment, as the corresponding reference product, Seebri Breezhaler, remains authorised
and available on the market. Patients taking Enurev Breezhaler or participating in a clinical trial are advised to consult their physician.

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Product information

български (BG) (736.6 Ko - PDF)

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español (ES) (678.02 Ko - PDF)

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čeština (CS) (734.47 Ko - PDF)

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dansk (DA) (680.69 Ko - PDF)

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Deutsch (DE) (713.25 Ko - PDF)

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eesti (ET) (676.05 Ko - PDF)

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ελληνικά (EL) (747.42 Ko - PDF)

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Latest procedure affecting product information:VR/0000320523
23/01/2026
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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).

español (ES) (106.35 Ko - PDF)

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čeština (CS) (112.53 Ko - PDF)

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dansk (DA) (105.65 Ko - PDF)

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Deutsch (DE) (107.2 Ko - PDF)

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eesti (ET) (106.42 Ko - PDF)

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ελληνικά (EL) (116.72 Ko - PDF)

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français (FR) (107.46 Ko - PDF)

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hrvatski (HR) (110.09 Ko - PDF)

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italiano (IT) (105.23 Ko - PDF)

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latviešu (LV) (110.31 Ko - PDF)

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lietuvių (LT) (109.63 Ko - PDF)

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magyar (HU) (110.9 Ko - PDF)

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Malti (MT) (110.62 Ko - PDF)

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Nederlands (NL) (104.19 Ko - PDF)

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polski (PL) (111.26 Ko - PDF)

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português (PT) (106.91 Ko - PDF)

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română (RO) (151.43 Ko - PDF)

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slovenčina (SK) (111.62 Ko - PDF)

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slovenščina (SL) (108.32 Ko - PDF)

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suomi (FI) (106.15 Ko - PDF)

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svenska (SV) (105.73 Ko - PDF)

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Íslenska (IS) (108.22 Ko - PDF)

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norsk (NO) (106.13 Ko - PDF)

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Product details

Name of medicine
Enurev Breezhaler
Active substance
glycopyrronium bromide
International non-proprietary name (INN) or common name
glycopyrronium bromide
Therapeutic area (MeSH)
Pulmonary Disease, Chronic Obstructive
Anatomical therapeutic chemical (ATC) code
R03BB06

Pharmacotherapeutic group

Drugs for obstructive airway diseases

Therapeutic indication

Enurev Breezhaler is indicated as a maintenance bronchodilator treatment to relieve symptoms in adult patients with chronic obstructive pulmonary disease (COPD).

Authorisation details

EMA product number
EMEA/H/C/002691
Marketing authorisation holder
Novartis Europharm Ltd

Novartis Europharm Limited
Elm Park
Merrion Road
Dublin 4
Ireland

Marketing authorisation issued
28/09/2012
Withdrawal of marketing authorisation
30/08/2026
Revision
12

Assessment history

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