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


Nurofen Cold & Flu Film-coated Tablets Ibuprofen 200mg Pseudophedrine hydrochloride 30mg



Reckitt Benckiser Ireland LtdPA0979/033/001

Main Information

Trade NameNurofen Cold & Flu Film-coated Tablets Ibuprofen 200mg Pseudophedrine hydrochloride 30mg
Active SubstancesIbuprofen
PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage FormFilm-coated tablet
Licence HolderReckitt Benckiser Ireland Ltd
Licence NumberPA0979/033/001

Group Information

ATC CodeM01AE Propionic acid derivatives
M01AE51 ibuprofen, combinations

Status

License statusAuthorised
Licence Issued18/04/1994
Legal statusProduct not subject to medical prescription
Supply StatusSupply through pharmacies only
Advertising StatusAdvertising to the general public
Conditions of LicenceSale through pharmacies only in packs containing not more than 24 units per pack. Packs containing more than 720mg pseudoephedrine are subject to medical prescription.
Marketing StatusMarketed

Documents

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