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


Mebeverine hydrochloride 135 mg Film-coated Tablets



Azure Pharmaceuticals Ltd.PA22871/006/001

Main Information

Trade NameMebeverine hydrochloride 135 mg Film-coated Tablets
Active SubstancesMebeverine hydrochloride
Dosage FormFilm-coated tablet
Licence HolderAzure Pharmaceuticals Ltd.
Licence NumberPA22871/006/001

Group Information

ATC CodeA03AA04 mebeverine

Status

License statusAuthorised
Licence Issued22/11/2019
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 StatusMarketed

Documents

Summary of Product CharacteristicsPDF Version
Package LeafletPDF Version
Public Assessment ReportNo document available
« Back