Dexrazoxane

Savene 500 mg, poeder en oplosmiddel voor oplossing voor infusie

Oplosmiddel voor parenteraal gebruik, Poeder voor oplossing voor injectieNetherlandsAuthorisedAuthorised 28 Jul 2006

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In other countries

The same active substances on other registers, the same brand first.

Authorised centrally in the EU

This national listing belongs to a medicine the European Commission authorised for the whole EU.

SaveneEuropean UnionAuthorised

SAVENE 20 mg/ml POLVO PARA CONCENTRADO Y DISOLVENTE PARA SOLUCION PARA PERFUSIONSpain · 20 mg · polvo y disolvente para concentrado para solución para perfusión · Cnx Therapeutics Ireland LimitedSame brand
SaveneEuropean Union · CNX Therapeutics Ireland LimitedSame brand
SaveneCroatiaSame brand
SaveneItaly · Soluzione per infusione · CNX Therapeutics Ireland LimitedSame brand
CARDIOXANE 500 mg POLVO PARA SOLUCION PARA PERFUSIONSpain · 500 mg · polvo para solución para perfusión · Cnx Therapeutics Ireland LimitedSame form

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Dexrazoxane

Savene 500 mg, poeder en oplosmiddel voor oplossing voor infusie

Oplosmiddel voor parenteraal gebruik, Poeder voor oplossing voor injectieNetherlandsAuthorisedAuthorised 28 Jul 2006

Product informationAsk Osler about it

In other countries

The same active substances on other registers, the same brand first.

Authorised centrally in the EU

This national listing belongs to a medicine the European Commission authorised for the whole EU.

SaveneEuropean UnionAuthorised

Two medicines in one question?

Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.

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CardioxaneItaly · Polvere per soluzione per infusione endovenosa · CNX Therapeutics Ireland Limited

e.g. CardioxaneNew Zealand · Inj 500 mg

Dexrazoxane HydrochlorideUnited States · 250MG BASE/VIAL, 500MG BASE/VIAL · injectable · MSN

TotectUnited States · 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · injectable · Clinigen

ZinecardUnited States · 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · injectable · Pfizer

CardioxaneBrazil · Adium S.A.

Dexrazoxane for InjectionCanada · 250 MG / VIAL · Powder For Solution · Juno Pharma Canada INC.

Dexrazoxane for InjectionCanada · 250 MG / VIAL · Powder For Solution · Hikma Canada Limited

ZinecardCanada · 250 MG / VIAL · Powder For Solution · Pfizer Canada Ulc

Documents

The official texts, at the regulator.

Sources and licences

Compiled by Prognia from the public register below; the register’s text is the official one.

College ter Beoordeling van Geneesmiddelen

College ter Beoordeling van Geneesmiddelen, Geneesmiddeleninformatiebank metadata, source update 07-10-2026; downloaded 08-10-2026; factual adaptation.

Licence: Conditional noncreative administrative factual metadata; no dataset-wide CC0 claim · Added 8 Oct 2026

Report an error or request removalCorrections from the holder or the register are welcome.

Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.

At a glance

Active substance: Dexrazoxane
Dosage form: Oplosmiddel voor parenteraal gebruik, Poeder voor oplossing voor injectie
Route: Intraveneus gebruik
Register: Netherlands (CBG-MEB)
Status: Authorised
Status in the register: Ingeschreven
Authorised: 28 Jul 2006
Registration: EU/1/06/350
Marketing authorisation holder: CNX Therapeutics Ireland Limited
ATC code: V03AF02
Group: Various
Procedure: EU centralised
Supply: Uitsluitend recept
EMA product number: EMEA/H/C/000682
EU number: EU/1/06/350