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Pharmaceuticals - Community Register


Community register of medicinal products for human use


Product information

Invented name: Ultibro Breezhaler   
Auth. number : EU/1/13/862
Active substance : indacaterol/glycopyrronium bromide
ATC: Anatomical main group: R - Respiratory system
Therapeutic subgroup: R03 - Anti-asthmatics
Pharmacological subgroup: R03A - Adrenergics, inhalants
Chemical subgroup: R03AL - Adrenergics in combination with anticholinergics
Chemical substance: R03AL04 - indacaterol and glycopyrronium bromide
(See WHO ATC Index)
Indication: Maintenance bronchodilator treatment to relieve symptoms in adult patients with chronic obstructive pulmonary disease (COPD).
Marketing Authorisation Holder: Novartis Europharm Limited
Frimley Business Park, Camberley GU16 7SR, United Kingdom
EPAR and active package presentations

Package presentations

Information about presentations can be found in the website of the European Medicines Agency under the section "Product Information".
Likewise, presentations on which there has been a Commission decision are referred in the Summary of Product Characteristics (Annex I to the Commission Decision granting the marketing authorisation) which is available in the Community Register.

European Commission proceduresGoto top of the page

Close date procedure Procedure type EMEA number Decision summary publ decision docs annex
23/09/2013 Centralised - Authorisation EMEA/H/C/2679 (2013)6229 of 19/09/2013
23/01/2014 Centralised - Variation EMEA/H/C/2679/WS/482
Updated with Decision(2014)10079 of 16/12/2014
18/12/2014 PSUSA - Modification EMEA/H/C/2679/PSUV/3 (2014)10079 of 16/12/2014
21/01/2015 Centralised - Variation EMEA/H/C/2679/IG/518
Updated with Decision(2016)632 of 28/01/2016
9/10/2015 Centralised - Variation EMEA/H/C/2679/IB/10/G
Updated with Decision(2016)632 of 28/01/2016
1/02/2016 Centralised - Yearly update (2016)632 of 28/01/2016
27/10/2016 Centralised - Variation EMEA/H/C/2679/WS/1004
Updated with Decision(2017)7400 of 30/10/2017
10/11/2016 Centralised - Variation EMEA/H/C/2679/WS/1005
Updated with Decision(2017)7400 of 30/10/2017
24/10/2017 Centralised - Variation EMEA/H/C/2679/IB/19/G
Updated with Decision(2018)3259 of 22/05/2018
1/11/2017 Centralised - Yearly update (2017)7400 of 30/10/2017
24/05/2018 Centralised - Renewal EMEA/H/C/2679/R/24 (2018)3259 of 22/05/2018