PANADOL EXTRA

500/65 Milligram Film Coated Tablet

GlaxoSmithKline Consumer Healthcare (Ireland) LimitedPA0678/027/001

Main Information

Trade NamePANADOL EXTRA
Active SubstancesPARACETAMOL
CAFFEINE
Strength500/65 Milligram
Dosage FormFilm Coated Tablet
Licence HolderGlaxoSmithKline Consumer Healthcare (Ireland) Limited
Licence NumberPA0678/027/001

Group Information

ATC CodeN02BE51 Analgesics and antipyretics

Status

Authorised/WithdrawnAuthorised
Licence Issued14/06/1994
Supply StatusSupply through general sales
Dispensing StatusProduct not subject to medical prescription
Marketing StatusMarketed
Promotion StatusPromotion to the general public
Conditions of LicenceGeneral Sale: MAXIMUM PACK SIZE 12. Contains only paracetamol as analgesic. Maximum one pack per sale. Pharmacy only: MAXIMUM PACK SIZE 24. Maximum two packs per sale. Prescription only: Pack size greater than 24. Product not supplied in blister packs. Promotion to the public: Pack size not more than 24 Promotion to healthcare professionals: Pack size greater than 24

Documents

Summary of Product CharacteristicsPDF Version
Package LeafletPDF Version
Public Assessment ReportPDF Version
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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.