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EMA Product

Brimica Genuair

Product approved by European Medicines Agency (EU)

Basic Information

Brimica Genuair

Regulatory Information

EMEA/H/C/003969

Authorised

November 19, 2014

16

June 20, 2024

Company Information

the netherlands

Gustav Mahlerplein 2 1082 MA Amsterdam

Covis Pharma Europe BV

Active Substances Detail

formoterol fumarate dihydrateaclidinium bromide

Detailed Information

Therapeutic Indication

### Therapeutic indication Brimica Genuair is indicated as a maintenance bronchodilator treatment for airflow obstruction and relief of symptoms in adult patients with chronic obstructive pulmonary disease (COPD).

Overview Summary

This is a summary of the European public assessment report (EPAR) for Brimica Genuair. It explains how the Agency assessed the medicine to recommend its authorisation in the EU and its conditions of use. It is not intended to provide practical advice on how to use Brimica Genuair. For practical information about using Brimica Genuair, patients should read the package leaflet or contact their doctor or pharmacist.

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