The HPRA advises healthcare professionals not to retain printed versions of Summary of Product Characteristics (SPC) documents. As these documents are subject to frequent content updates, including changes to safety and dose related information, we recommend that you visit our website as necessary to access the most up-to-date versions. If you have any queries about specific SPCs on our website then please e-mail info@hpra.ie


CLOPIDOGREL TEVA



Teva B.V.EU/1/09/540/1-16

Main Information

Trade NameCLOPIDOGREL TEVA
Active SubstancesCLOPIDOGREL HYDROGEN SULPHATE
Dosage FormFilm-coated tablet
Licence HolderTeva B.V.
Licence NumberEU/1/09/540/1-16

Group Information

ATC CodeB01AC04 clopidogrel

Status

License statusAuthorised
Licence Issued28/07/2009
Legal statusProduct subject to prescription which may be renewed (B)
Supply StatusSupply through pharmacies only
Advertising StatusAdvertising to healthcare professionals only
Conditions of Licence
Marketing Status

Documents

Summary of Product CharacteristicsSearch EMA website
Package LeafletSearch EMA website
Public Assessment ReportSearch EMA website

Generics Information

Interchangeable List CodeIC0005-028-003
Interchangeable List DocumentPDF of Interchangeable List
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