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IBUPROFEN AND CODEINE 200 MG/ 12.8 MG FILM-COATED

200/12.8 Milligram Film Coated Tablet

Reckitt Benckiser Ireland LtdPA0004/066/001

Main Information

Trade NameIBUPROFEN AND CODEINE 200 MG/ 12.8 MG FILM-COATED
Active SubstancesIBUPROFEN
CODEINE PHOSPHATE HEMIHYDRATE
Strength200/12.8 Milligram
Dosage FormFilm Coated Tablet
Licence HolderReckitt Benckiser Ireland Ltd
Licence NumberPA0004/066/001

Group Information

ATC CodeN02AJ08 codeine and ibuprofen

Status

Authorised/WithdrawnAuthorised
Licence Issued17/12/2010
Supply StatusSupply through pharmacies only
Dispensing StatusProduct not subject to medical prescription
Marketing StatusMarketed
Promotion StatusPromotion to Healthcare Professionals only
Conditions of LicenceProduct not subject to medical prescription, supply through pharmacies only and promotion to the healthcare professionals only subject to the following restrictions: For ibuprofen: maximum strength 200 mg, maximum dose: 400 mg, maximum daily dose 1200 mg, limited indications. For use in adults

Documents

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