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


Brilique



AstraZeneca ABEU/1/10/655/007-011

Main Information

Trade NameBrilique
Active SubstancesTicagrelor
Dosage FormFilm-coated tablet
Licence HolderAstraZeneca AB
Licence NumberEU/1/10/655/007-011

Group Information

ATC CodeB01AC24 ticagrelor

Status

License statusAuthorised
Licence Issued18/02/2016
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 StatusUnknown

Documents

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