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Oramox 125 mg/5 ml Powder for Oral Suspension



Athlone Pharmaceuticals LimitedPA1418/013/001

Main Information

Trade NameOramox 125 mg/5 ml Powder for Oral Suspension
Active SubstancesAmoxicillin trihydrate
Dosage FormPowder for oral suspension
Licence HolderAthlone Pharmaceuticals Limited
Licence NumberPA1418/013/001

Group Information

ATC CodeJ01CA Penicillins with extended spectrum
J01CA04 amoxicillin

Status

License statusAuthorised
Licence Issued27/09/1988
Legal statusProduct subject to prescription which may not be renewed (A)
Supply StatusSupply through pharmacies only
Advertising StatusAdvertising to healthcare professionals only
Conditions of LicenceThis authorisation permits the holder to market only product authorised in Ireland under the PA1418/013/001.
Marketing StatusMarketed

Documents

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