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

Cefuroxime 750 mg Powder for solution for injection

Stravencon LtdPA1947/002/002

Main Information

Trade NameCefuroxime 750 mg Powder for solution for injection
Active SubstancesCefuroxime Sodium
Dosage FormPowder for solution for injection
Licence HolderStravencon Ltd
Licence NumberPA1947/002/002

Group Information

ATC CodeJ01DC Second-generation cephalosporins
J01DC02 cefuroxime


License statusAuthorised
Licence Issued13/08/2015
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 StatusNot marketed


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