01 2Aurobindo Pharma Limited
02 3CNX Therapeutics
03 3Clinigen Group
04 2GLAND PHARMA LIMITED
05 2Hikma Pharmaceuticals
06 1JUNO PHARMACEUTICALS CORP.
07 2MSN Laboratories
08 1Novartis Pharmaceuticals Corporation
09 3Pfizer Inc
01 1Dexrazoxano 500Mg 1 Unit Parenteral Use
02 11INJECTABLE;INJECTION
03 2POWDER FOR SOLUTION
04 1Powder For Concentrate And Solvent For Infusion Solution
05 1Powder For Infusion Solution
06 1Powder to concentrate and liquid to the infusion fluid, resolution
07 2Solution For Injection
01 1Approved
02 2Authorized
03 3DISCN
04 1Deregistered
05 2Prescription
06 8RX
07 2Blank
01 3Cardioxane
02 1DEXRAZOXANE FOR INJECTION
03 8DEXRAZOXANE HYDROCHLORIDE
04 3Savene
05 1TOTECT
06 3ZINECARD
01 2Canada
02 1Italy
03 1Norway
04 2Spain
05 2Sweden
06 11USA
Regulatory Info : RX
Registration Country : USA
Brand Name : DEXRAZOXANE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 250MG BASE/VIAL
Packaging :
Approval Date : 2011-10-19
Application Number : 200752
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : DEXRAZOXANE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2011-10-19
Application Number : 200752
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TOTECT
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2007-09-06
Application Number : 22025
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Italy
Brand Name : Cardioxane
Dosage Form : Dexrazoxano 500Mg 1 Unit Parenteral Use
Dosage Strength : 1 ampoule EV 500 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Norway
Brand Name : Savene
Dosage Form : Powder to concentrate and liquid to the infusion fluid, resolution
Dosage Strength : 20 mg/ml
Packaging : Set
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Savene
Dosage Form : Solution For Injection
Dosage Strength : 20mg/ml
Packaging :
Approval Date : 28/07/2006
Application Number : 20050924000017
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Cardioxane
Dosage Form : Powder For Infusion Solution
Dosage Strength : 500MG
Packaging :
Approval Date : 2006-03-31
Application Number : 67673
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Savene
Dosage Form : Powder For Concentrate And Solvent For Infusion Solution
Dosage Strength : 20MG
Packaging :
Approval Date : 2007-02-21
Application Number : 06350001
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : RX
Registration Country : USA
Brand Name : DEXRAZOXANE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2016-11-28
Application Number : 207321
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : DEXRAZOXANE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 250MG BASE/VIAL
Packaging :
Approval Date : 2019-12-16
Application Number : 207321
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : DEXRAZOXANE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 250MG BASE/VIAL
Packaging :
Approval Date : 2004-09-28
Application Number : 76068
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : DEXRAZOXANE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2004-09-28
Application Number : 76068
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : DEXRAZOXANE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 250MG BASE/VIAL
Packaging :
Approval Date : 2025-03-26
Application Number : 216748
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : DEXRAZOXANE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2025-03-26
Application Number : 216748
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Cardioxane
Dosage Form : Solution For Injection
Dosage Strength : 500mg
Packaging :
Approval Date : 05/07/2006
Application Number : 20051011000019
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ZINECARD
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1995-05-26
Application Number : 20212
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ZINECARD
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1995-05-26
Application Number : 20212
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : ZINECARD
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 250MG/VIAL
Packaging : 250MG/25ML VIAL
Approval Date :
Application Number : 2153432
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : DEXRAZOXANE FOR INJECTION
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 250MG/VIAL
Packaging :
Approval Date :
Application Number : 2544083
Regulatory Info : Prescription
Registration Country : Canada
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