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


Tramadol Hydrochloride/Paracetamol 37.5mg/325mg Film-Coated Tablets

37.5/325 milligram(s) Film-coated tablet

Athlone Laboratories LtdPA0298/024/001

Main Information

Trade NameTramadol Hydrochloride/Paracetamol 37.5mg/325mg Film-Coated Tablets
Active SubstancesParacetamol
Tramadol hydrochloride
Strength37.5/325 milligram(s)
Dosage FormFilm-coated tablet
Licence HolderAthlone Laboratories Ltd
Licence NumberPA0298/024/001

Group Information

ATC CodeN02AX Other opioids
N02AX52 tramadol, combinations

Status

Authorised/WithdrawnAuthorised
Licence Issued10/06/2016
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 StatusNot marketed

Documents

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

Generics Information

Interchangeable List CodeIC0077-133-014
Interchangeable List DocumentPDF of Interchangeable List
« Back