NUROFEN

200 Milligram Coated Tablets

Reckitt Benckiser Ireland LtdPA0979/032/006

Main Information

Trade NameNUROFEN
Active SubstancesIBUPROFEN
Strength200 Milligram
Dosage FormCoated Tablets
Licence HolderReckitt Benckiser Ireland Ltd
Licence NumberPA0979/032/006

Group Information

ATC CodeM01AE01 Propionic acid derivatives

Status

Authorised/WithdrawnAuthorised
Licence Issued16/02/2007
Supply StatusSupply through pharmacies only
Dispensing StatusProduct not subject to medical prescription
Marketing StatusMarketed
Promotion StatusPromotion to the general public
Conditions of LicenceSupply through pharmacies only if compliant with the following restrictions: maximum strength: 200 mg; maximum pack size 50; maximum dose: 400 mg; maximum daily dose 1200 mg; limited indications. Promotion to the public if compliant with the following restrictions: maximum strength: 200 mg; maxim

Documents

Summary of Product CharacteristicsPDF Version
Package LeafletPDF Version
Public Assessment ReportPDF Version
« Back

Latest Changes to Medicine Info & SPC

View all available

Please note changes to the medicine information and summary of product characteristics are only available from the 19/05/2015 onwards. Changes made before this date aren't available online.