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Prednisolone 20 mg Rectal Foam



Chemidex Pharma LimitedPA22643/003/001

Main Information

Trade NamePrednisolone 20 mg Rectal Foam
Active SubstancesPrednisolone
Dosage FormRectal foam
Licence HolderChemidex Pharma Limited
Licence NumberPA22643/003/001

Group Information

ATC CodeD07AA Corticosteroids, weak (group I)
D07AA03 prednisolone

Status

License statusAuthorised
Licence Issued11/02/2011
Legal statusProduct subject to prescription which may not be renewed (A)
Supply StatusSupply through pharmacies only
Advertising StatusAdvertising to healthcare professionals only
Conditions of Licence
Marketing StatusMarketed

Documents

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