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01 1Aurobindo Pharma Limited
02 2Clinigen Group
03 2Cosette Pharma
04 1Merck & Co
05 1Pinnacle Biologics
06 1Sun Pharmaceutical Industries Limited
07 1TherDose Pharma
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01 1Amifostine 500Mg 3 Units' Parenteral Use
02 1INJ
03 4INJECTABLE;INJECTION
04 1Injection
05 1Powder For Infusion Solution
06 1Solution For Injection
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01 1Cancelled
02 4DISCN
03 1Deregistered
04 1Originator
05 2Blank
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01 1AMFOSTED
02 2AMIFOSTINE
03 2ETHYOL
04 4Ethyol
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01 1India
02 1Italy
03 1South Africa
04 1Spain
05 1Sweden
06 4USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : AMIFOSTINE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 500MG/VIAL
Packaging :
Approval Date : 2017-07-17
Application Number : 204363
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Italy
Brand Name : Ethyol
Dosage Form : Amifostine 500Mg 3 Units' Parenteral Use
Dosage Strength : 3 vials groun EV 500 mg 50 mg/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Ethyol
Dosage Form : Powder For Infusion Solution
Dosage Strength : 50MG
Packaging :
Approval Date : 1996-02-01
Application Number : 60650
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ETHYOL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1995-12-08
Application Number : 20221
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ETHYOL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 375MG/VIAL
Packaging :
Approval Date : 1999-09-10
Application Number : 20221
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Ethyol
Dosage Form : INJ
Dosage Strength : 500mg
Packaging : 3X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Ethyol
Dosage Form : Solution For Injection
Dosage Strength : 50mg/ml
Packaging :
Approval Date : 29/05/1998
Application Number : 19980529000164
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : DISCN
Registration Country : USA
Brand Name : AMIFOSTINE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 500MG/VIAL
Packaging :
Approval Date : 2008-03-14
Application Number : 77126
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : India
Brand Name : AMFOSTED
Dosage Form : Injection
Dosage Strength : 500mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India