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

Viartril 1500 mg Powder for Oral Solution

Rottapharm LtdPA0868/005/001

Main Information

Trade NameViartril 1500 mg Powder for Oral Solution
Active SubstancesGlucosamine sulphate sodium chloride
Dosage FormPowder for oral solution
Licence HolderRottapharm Ltd
Licence NumberPA0868/005/001

Group Information

ATC CodeM01AX Other antiinflammatory and antirheumatic agents, non-steroids
M01AX05 glucosamine


License statusAuthorised
Licence Issued08/07/2005
Legal statusProduct not subject to medical prescription
Supply StatusSupply through pharmacies only
Advertising StatusAdvertising to the general public
Conditions of LicenceThis authorisation permits the holder to market only product authorised in Ireland under the product authorisation number PA868/1/1.
Marketing StatusNot marketed


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