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Cerubidin 20 mg Powder for Concentrate for Solution for Infusion

20 milligram(s) Pdr/Conc/Soln for Infus

Sanofi-Aventis Ireland Limited T/A SANOFIPA0540/096/001

Main Information

Trade NameCerubidin 20 mg Powder for Concentrate for Solution for Infusion
Active SubstancesDaunorubicin hydrochloride
Strength20 milligram(s)
Dosage FormPdr/Conc/Soln for Infus
Licence HolderSanofi-Aventis Ireland Limited T/A SANOFI
Licence NumberPA0540/096/001

Group Information

ATC CodeL01DB Anthracyclines and related substances
L01DB02 daunorubicin

Status

Authorised/WithdrawnAuthorised
Licence Issued20/04/1995
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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