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Panadol Original 500 mg film-coated Tablets



Haleon Ireland LimitedPA0678/039/005

Main Information

Trade NamePanadol Original 500 mg film-coated Tablets
Active SubstancesParacetamol
Dosage FormFilm-coated tablet
Licence HolderHaleon Ireland Limited
Licence NumberPA0678/039/005

Group Information

ATC CodeN02BE Anilides
N02BE01 paracetamol

Status

License statusAuthorised
Licence Issued01/04/1978
Legal statusProduct not subject to medical prescription
Supply StatusSupply through non-pharmacy outlets and pharmacies
Advertising StatusAdvertising to the general public
Conditions of Licence As an item for general sale in a maximum pack size of 12 tablets supplied in blister packs only. Only one pack should be supplied on each occasion of purchase. As an item for retail sale through pharmacies only in blister packs containing not more than 24 tablets. Not more than two such packs should be supplied to a single patient unless a valid prescription exists. Packs containing more than 24 tablets may be supplied to pharmacies for use by pharmacists provided the label states that they are for dispensing purposes only. As a prescription only item in packs containing more than 50 tablets. 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 StatusNot marketed

Documents

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