01 2Aurobindo Pharma Limited
02 4Clinigen Group
03 2GLAND PHARMA LIMITED
04 2Hikma Pharmaceuticals
05 3Pfizer Inc
01 1Dexrazoxano 500Mg 1 Unit Parenteral Use
02 9INJECTABLE;INJECTION
03 1POWDER FOR CONCENTRATE AND SOLVENT
04 1POWDER FOR SOLUTION
05 1Powder to concentrate and liquid to the infusion fluid, resolution
01 3DISCN
02 1Prescription
03 6RX
04 3Blank
01 1Cardioxane
02 6DEXRAZOXANE HYDROCHLORIDE
03 2Savene
04 1TOTECT
05 3ZINECARD
01 1Canada
02 1Italy
03 1Norway
04 1Sweden
05 9USA
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Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : Sweden
Brand Name : Savene
Dosage Form : POWDER FOR CONCENTRATE AND SOLVENT
Dosage Strength : 20 MG / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
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 : 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 : DISCN
Registration Country : USA
Brand Name : ZINECARD
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 250MG BASE/VIAL
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
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
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