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Paracetamol 500 mg Film Coated Tablets



GlaxoSmithKline Consumer Healthcare (Ireland) LimitedPA0678/150/001

Main Information

Trade NameParacetamol 500 mg Film Coated Tablets
Active SubstancesParacetamol
Dosage FormFilm-coated tablet
Licence HolderGlaxoSmithKline Consumer Healthcare (Ireland) Limited
Licence NumberPA0678/150/001

Group Information

ATC CodeN02BE Anilides
N02BE01 paracetamol

Status

License statusAuthorised
Licence Issued02/03/1989
Legal statusProduct not subject to medical prescription
Supply StatusSupply through non-pharmacy outlets and pharmacies
Advertising StatusAdvertising to the general public
Conditions of LicenceGeneral sale in blister packs containing not more than 12 unit dosage forms. Only one pack should be supplied in the course of any one retail transaction. Retail sale through pharmacies only in blister packs containing not more than 24 unit dosage forms. Not more than two such packs should be supplied in the course of any one retail transaction unless a valid prescription exists. Packs containing more than 24 unit dosage forms may be supplied to pharmacies for use by pharmacists provided the label states that they are for dispensing purposes only. Packs containing more than 50 unit dosage forms are prescription only. Promotion to the general public for packs containing not more than 24 unit dosage forms. Promotion to healthcare professionals only for packs containing more than 24 unit dosage forms.
Marketing StatusMarketed

Documents

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