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


IRBESARTAN/HYDROCHLOROTHIAZIDE TEVA



Teva B.V.EU/1/09/583/25-48

Main Information

Trade NameIRBESARTAN/HYDROCHLOROTHIAZIDE TEVA
Active SubstancesIRBESARTAN
HYDROCHLOROTHIAZIDE, MICRONISED
Dosage FormFilm-coated tablet
Licence HolderTeva B.V.
Licence NumberEU/1/09/583/25-48

Group Information

ATC CodeC09DA04 irbesartan and diuretics

Status

License statusAuthorised
Licence Issued26/11/2009
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
« Back