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


Tylex 30 mg / 500 mg Effervescent Tablets

30 mg/500 milligram(s) Effervescent tablet

UCB (Pharma) Ireland LimitedPA0891/014/002

Main Information

Trade NameTylex 30 mg / 500 mg Effervescent Tablets
Active SubstancesCodeine phosphate hemihydrate
Paracetamol
Strength30 mg/500 milligram(s)
Dosage FormEffervescent tablet
Licence HolderUCB (Pharma) Ireland Limited
Licence NumberPA0891/014/002

Group Information

ATC CodeN02AJ Opioids in combination with non-opioid analgesics
N02AJ06 codeine and paracetamol

Status

Authorised/WithdrawnAuthorised
Licence Issued22/10/1996
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
« Back