Clopidogrel DURA (clopidogrel)
Generic
- Region
- 🇪🇺 EU
- Active substance
- clopidogrel
- Company
- Mylan dura GmbH
- Status
- Withdrawn
- Therapeutic area
- Peripheral Vascular Diseases; Stroke; Myocardial Infarction
- EU approval
- Tue 21 Jul 2009
- Designations
- Generic
- Application
- EMEA/H/C/001132
- ATC
- B01AC04
- Official record
- www.ema.europa.eu
Indication
Clopidogrel is indicated in adults for the prevention of atherothrombotic events in: Patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease.
Regulatory milestones
No milestones recorded in the last year.
Same substance in other markets
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- 🇪🇺 Iscover Authorised · Sanofi Winthrop Industrie
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- 🇪🇺 Grepid Authorised · Pharmathen S.A.
- 🇪🇺 Clopidogrel Krka Authorised · KRKA tovarna zdravil d.d. Novo mesto
- 🇪🇺 Clopidogrel Krka d.d. (previously Zopya) Authorised · Norpharm Regulatory Services Ltd
- 🇪🇺 Clopidogrel TAD Authorised · Tad Pharma GmbH
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- 🇪🇺 Clopidogrel / Acetylsalicylic acid Viatris (previously Clopidogrel / Acetylsalicylic acid Mylan) Authorised · Mylan Pharmaceuticals Limited
- 🇪🇺 Clopidogrel ratiopharm Authorised · Teva B.V.
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