The HPRA advises healthcare professionals not to retain printed versions of Summary of Product Characteristics (SPC) documents. As these documents are subject to frequent content updates, including changes to safety and dose related information, we recommend that you visit our website as necessary to access the most up-to-date versions. If you have any queries about specific SPCs on our website then please e-mail info@hpra.ie


Panadol Soluble Max 1000mg Paracetamol Effervescent granules



Haleon Ireland LimitedPA0678/028/002

Main Information

Trade NamePanadol Soluble Max 1000mg Paracetamol Effervescent granules
Active SubstancesParacetamol
Dosage FormEffervescent granules
Licence HolderHaleon Ireland Limited
Licence NumberPA0678/028/002

Group Information

ATC CodeN02BE Anilides
N02BE01 paracetamol

Status

License statusAuthorised
Licence Issued20/08/1992
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 packs containing not more than 6 individual unit dosage forms. Only one pack should be supplied in the course of any one retail transaction. Retail sale through pharmacies only in packs containing not more than 12 individual 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 12 individual unit dosage forms are prescription only. promotion to the general public for packs containing not more than 12 unit dosage forms. Promotion to healthcare professionals only for packs containing more than 12 unit dosage forms.
Marketing StatusNot marketed

Documents

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