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


Augmentin 500 mg/125 mg Film-coated Tablets

500/125 milligram(s) Film-coated tablet

Imbat LimitedPPA1151/050/003

Main Information

Trade NameAugmentin 500 mg/125 mg Film-coated Tablets
Active SubstancesAmoxicillin trihydrate
Potassium clavulanate
Strength500/125 milligram(s)
Dosage FormFilm-coated tablet
Licence HolderImbat Limited
Licence NumberPPA1151/050/003

Group Information

ATC CodeJ01CR02 amoxicillin and enzyme inhibitor

Status

Authorised/WithdrawnAuthorised
Licence Issued06/08/2010
Legal statusProduct subject to prescription which may not be renewed (A)
Supply StatusSupply through pharmacies only
Advertising StatusAdvertising to healthcare professionals only
Conditions of Licence
Marketing StatusUnknown

Documents

Summary of Product CharacteristicsPDF Version
Package LeafletNo document available
Public Assessment ReportNo document available

Generics Information

Interchangeable List CodeIC0037-073-003
Interchangeable List DocumentPDF of Interchangeable List
« Back