Clopidogrel/Acetylsalicylic acid Zentiva (previously DuoCover)
clopidogrel / acetylsalicylic acid
Table of contents
Overview
This document is a summary of the European Public Assessment Report (EPAR) for Clopidogrel/Acetylsalicylic acid Zentiva. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Clopidogrel/Acetylsalicylic acid Zentiva.
Authorisation details
Product details | |
---|---|
Name |
Clopidogrel/Acetylsalicylic acid Zentiva (previously DuoCover)
|
Agency product number |
EMEA/H/C/001144
|
Active substance |
|
International non-proprietary name (INN) or common name |
|
Therapeutic area (MeSH) |
|
Anatomical therapeutic chemical (ATC) code |
B01AC30
|
Publication details | |
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Marketing-authorisation holder |
Sanofi-Aventis Groupe
|
Revision |
22
|
Date of issue of marketing authorisation valid throughout the European Union |
14/03/2010
|
Contact address |
54 rue La Boétie
F-75008 Paris France |
Product information
19/09/2019 Clopidogrel/Acetylsalicylic acid Zentiva (previously DuoCover) - EMEA/H/C/001144 - WS/1665
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).
You can find product information documents for centrally authorised human medicines on this website. For centrally authorised veterinary medicines authorised or updated from February 2022, see the Veterinary Medicines Information website.
Pharmacotherapeutic group
Antithrombotic agents
Therapeutic indication
- Acute Coronary Syndrome
- Myocardial Infarction