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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.

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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    Dexrazoxane

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    01 2Aurobindo Pharma Limited

    02 4Clinigen Group

    03 2GLAND PHARMA LIMITED

    04 2Hikma Pharmaceuticals

    05 3Pfizer Inc

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    Aurobindo Pharma Limited

    India
    2024 ACI Convention
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    Aurobindo Pharma Limited

    India
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    Regulatory Info : RX

    Registration Country : USA

    DEXRAZOXANE HYDROCHLORIDE

    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

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    02

    Aurobindo Pharma Limited

    India
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    Aurobindo Pharma Limited

    India
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    Regulatory Info : RX

    Registration Country : USA

    DEXRAZOXANE HYDROCHLORIDE

    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

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    03

    Clinigen Group

    United Kingdom
    2024 ACI Convention
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    Clinigen Group

    United Kingdom
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    Regulatory Info : DISCN

    Registration Country : USA

    DEXRAZOXANE HYDROCHLORIDE

    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**

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    Approval Date : 2007-09-06

    Application Number : 22025

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Clinigen Group

    United Kingdom
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    Regulatory Info :

    Registration Country : Sweden

    Dexrazoxane HCl

    Brand Name : Savene

    Dosage Form : POWDER FOR CONCENTRATE AND SOLVENT

    Dosage Strength : 20 MG / ML

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    Approval Date :

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    Registration Country : Sweden

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    05

    Clinigen Group

    United Kingdom
    2024 ACI Convention
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    Clinigen Group

    United Kingdom
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    Registration Country : Italy

    Dexrazoxane

    Brand Name : Cardioxane

    Dosage Form : Dexrazoxano 500Mg 1 Unit Parenteral Use

    Dosage Strength : 1 ampoule EV 500 mg

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    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Italy

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    06

    Clinigen Group

    United Kingdom
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    Regulatory Info :

    Registration Country : Norway

    Dexrazoxane

    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

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    07

    GLAND PHARMA LIMITED

    India
    2024 ACI Convention
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    GLAND PHARMA LIMITED

    India
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    Regulatory Info : RX

    Registration Country : USA

    DEXRAZOXANE HYDROCHLORIDE

    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

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    08

    GLAND PHARMA LIMITED

    India
    2024 ACI Convention
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    GLAND PHARMA LIMITED

    India
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    Regulatory Info : RX

    Registration Country : USA

    DEXRAZOXANE HYDROCHLORIDE

    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

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    09

    Hikma Pharmaceuticals

    United Kingdom
    2024 ACI Convention
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    Hikma Pharmaceuticals

    United Kingdom
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    Regulatory Info : RX

    Registration Country : USA

    DEXRAZOXANE HYDROCHLORIDE

    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

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    10

    Hikma Pharmaceuticals

    United Kingdom
    2024 ACI Convention
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    Virtual Booth Virtual Booth
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    Regulatory Info : RX

    Registration Country : USA

    DEXRAZOXANE HYDROCHLORIDE

    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

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    11

    Pfizer Inc

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    Pfizer Inc

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    DEXRAZOXANE HYDROCHLORIDE

    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

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    12

    Pfizer Inc

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    Pfizer Inc

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    DEXRAZOXANE HYDROCHLORIDE

    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

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    13

    Pfizer Inc

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    Pfizer Inc

    U.S.A
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    Regulatory Info : Prescription

    Registration Country : Canada

    DEXRAZOXANE

    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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