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MIRVASO Gel Ref  [6613] Active ingredients: Brimonidine Source: European Medicines Agency (EU) Revision Year: 2023 Publisher: Galderma International, Tour Europlaza, 20 avenue André Prothin – La Défense 4, La Défense Cedex 92927, FranceMirvaso offers patients an easy-to-apply, long-acting treatment with visible reductions in facial redness within 30 minutes of application — potentially giving them a better quality of life ' Marketing Authorisation in Europe for Mirvaso is applicable to the 28 Member States of the European Union, as well as Iceland, Lichtenstein and Norway Feb 20, 2014 · European Medicines Agency drug approval for Mirvaso by Unknown  View regulatory information and product details List of Marketing Authorisations (MA) of Mirvaso - Galderma, registered and approved in Europe on PharmaCompass comList of Marketing Authorisations (MA) containing mirvaso registered and approved in Europe on PharmaCompass com欧盟EMA药品数据库（European Medicines Agency Authorisation of Medicines DataBase）Feb 27, 2014 · The European Commission (EC) has granted marketing authorisation in Europe for Switzerland-based pharmaceutical firm Galderma's Mirvaso (brimonidine) 3mg g gel for the treatment of facial redness, also known as rosacea