01 1Aspen Pharmacare Holdings
02 1Akrikhin
03 1Epic Pharma. LLC.
04 1Flagship Biotech International Pvt. Ltd
05 4Macleods Pharmaceuticals Limited
06 1NORVIUM BIOSCIENCE
07 1Rajasthan Antibiotics
08 1Zhejiang Hisun Pharmaceutical
01 4DRY POWDER INJECTION
02 1INJ
03 3INJECTABLE;INJECTION
04 1Injection
05 1Lyophilised Injection
06 1Powder for Injection
01 3DISCN
02 1Generic
03 4Generic WHO/SRA/ERP Approved
04 1Originator
05 2Blank
01 1CAPASTAT SULFATE
02 2CAPREOMYCIN SULFATE
03 1Capastat 1 G
04 7Blank
01 2India
02 1Russia
03 1South Africa
04 3USA
05 4United Kingdom
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Capastat 1 G
Dosage Form : INJ
Dosage Strength : 1g
Packaging : 1X1g
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info :
Registration Country : Russia
Brand Name :
Dosage Form : Powder for Injection
Dosage Strength : 1000MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Russia
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CAPASTAT SULFATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50095
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Generic
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 1G
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Regulatory Info : Generic WHO/SRA/ERP Approved
Registration Country : United Kingdom
Brand Name :
Dosage Form : DRY POWDER INJECTION
Dosage Strength : 500MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic WHO/SRA/ERP Approved
Registration Country : United Kingdom
Regulatory Info : Generic WHO/SRA/ERP Approved
Registration Country : United Kingdom
Brand Name :
Dosage Form : DRY POWDER INJECTION
Dosage Strength : 750MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic WHO/SRA/ERP Approved
Registration Country : United Kingdom
Regulatory Info : Generic WHO/SRA/ERP Approved
Registration Country : United Kingdom
Brand Name :
Dosage Form : DRY POWDER INJECTION
Dosage Strength : 1000MG
Packaging :
Approval Date :
Application Number : 50095
Regulatory Info : Generic WHO/SRA/ERP Approved
Registration Country : United Kingdom
Regulatory Info : Generic WHO/SRA/ERP Approved
Registration Country : United Kingdom
Brand Name :
Dosage Form : DRY POWDER INJECTION
Dosage Strength : 2000MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic WHO/SRA/ERP Approved
Registration Country : United Kingdom
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Lyophilised Injection
Dosage Strength : 1G
Packaging : Vial
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CAPREOMYCIN SULFATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2018-10-18
Application Number : 204796
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CAPREOMYCIN SULFATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2017-11-27
Application Number : 202634
Regulatory Info : DISCN
Registration Country : USA
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