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01 1CLINIGEN HEALTHCARE LTD

02 1CNX Therapeutics Ireland Ltd.

03 3Cnx Therapeutics Ireland Limited

04 1Cnx Therapeutics Ireland Ltd

05 1Novartis Sweden Ab

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PharmaCompass

01

IPPE
Not Confirmed
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IPPE
Not Confirmed

Dexrazoxane

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

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02

IPPE
Not Confirmed
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IPPE
Not Confirmed

Dexrazoxane Hydrochloride

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

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03

IPPE
Not Confirmed
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IPPE
Not Confirmed

Dexrazoxane hydrochloride

Brand Name : The Saws

Dosage Form : Powder And Solvent For Concentrate For Solution For Infusion

Dosage Strength : 20mg/ml

Packaging :

Approval Date :

Application Number :

Regulatory Info : Marketed

Registration Country : Norway

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04

IPPE
Not Confirmed
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IPPE
Not Confirmed

Dexrazoxane

Brand Name : Savene

Dosage Form : Powder And Solvent For Concentrate For Solution For Infusion

Dosage Strength : 20mg/ml

Packaging :

Approval Date :

Application Number :

Regulatory Info : Prescription

Registration Country : Estonia

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05

IPPE
Not Confirmed
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IPPE
Not Confirmed

Dexrazoxane

Brand Name : Cardioxane

Dosage Form : Powder For Infusion Solution

Dosage Strength : 500MG

Packaging :

Approval Date : 31-03-2006

Application Number : 67673

Regulatory Info : Authorized

Registration Country : Spain

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06

IPPE
Not Confirmed
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IPPE
Not Confirmed

Dexrazoxane

Brand Name : Savene

Dosage Form : Powder For Concentrate And Solvent For Infusion Solution

Dosage Strength : 20MG

Packaging :

Approval Date : 21-02-2007

Application Number : 6350001

Regulatory Info : Authorized

Registration Country : Spain

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07

IPPE
Not Confirmed
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IPPE
Not Confirmed

Dexrazoxane Hydrochloride

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

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