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01 1Aspen Pharmacare Holdings
02 1Amnos Lifesciences
03 1Ascent Innovative Medicines
04 1Ebb Medical
05 2Eli Lilly
06 4Farbe Firma
07 1Fresenius Kabi Austria
08 2Fresenius Kabi USA
09 3Hikma Pharmaceuticals
10 1Hospira, Inc.
11 1Intelliscend
12 2Leo Pharma
13 3ORIFARM GROUP AS
14 1Omnia L?kemedel Ab
15 2Paranova Pharmaceuticals Ab
16 2Pfizer Inc
17 1Pharmachim Ab
18 2Quad Pharma
19 1Sandoz B2B
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01 1Ampoule
02 1INJ
03 1Injectable Solution
04 2Injectable; Injection
05 6Injection
06 2POWDER;INTRAVENOUS
07 2SOLUTION
08 7SOLUTION;INTRAVENOUS
09 1Solution
10 9Solution For Injection/Infusion
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01 2Approved
02 1Authorized
03 1Cancelled
04 7DISCN
05 7Deregistered
06 2Ethical
07 1Generic
08 2RX
09 9Blank
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01 11PROTAMINE SULFATE
02 1PROTAMINE SULFATE INJECTION USP
03 1PROTAMINE SULFATE INJECTION, USP
04 1Protamin
05 1Protamina Hospira
06 1Protamina Sulfato Leo Pharma
07 4Protamine Sulfate Leo Pharma
08 1Protamine Sulphate Injection B.P.
09 2Protamine Sulphate Leo Pharma
10 1Protaminsulfat Ebb
11 2Protaminsulfat Paranova
12 6Blank
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01 2Canada
02 7India
03 1South Africa
04 2Spain
05 9Sweden
06 11USA
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Protamine Sulphate Injection B.P.
Dosage Form : INJ
Dosage Strength : 50mg/5ml
Packaging : 5X10mg/5ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Ampoule
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 10MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROTAMINE SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 50MG/5ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 6460
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROTAMINE SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 250MG/25ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 6460
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 10MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 10MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 10MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 10MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : RX
Registration Country : USA
Brand Name : PROTAMINE SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 50MG/5ML (10MG/ML)
Packaging :
Approval Date : 1987-04-07
Application Number : 89454
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PROTAMINE SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 250MG/25ML (10MG/ML)
Packaging :
Approval Date : 1987-04-07
Application Number : 89454
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROTAMINE SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 50MG/5ML (10MG/ML)
Packaging :
Approval Date : 1986-11-05
Application Number : 89474
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROTAMINE SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 250MG/25ML (10MG/ML)
Packaging :
Approval Date : 1986-11-05
Application Number : 89475
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROTAMINE SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 50MG/5ML (10MG/ML)
Packaging :
Approval Date : 1988-06-07
Application Number : 89475
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : India
Brand Name : Protamin
Dosage Form : Injection
Dosage Strength : 10MG/1ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Protamine Sulfate Leo Pharma
Dosage Form : Solution For Injection/Infusion
Dosage Strength : 1400anti-heparinIU/ml
Packaging :
Approval Date : 04/08/2005
Application Number : 20040607004043
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROTAMINE SULFATE
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : 50MG/VIAL
Packaging :
Approval Date : 1982-01-01
Application Number : 7413
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROTAMINE SULFATE
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : 250MG/VIAL
Packaging :
Approval Date : 1984-08-02
Application Number : 7413
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : PROTAMINE SULFATE
Dosage Form : Injectable; Injection
Dosage Strength : 10MG/ML
Packaging :
Approval Date :
Application Number : 89306
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : PROTAMINE SULFATE
Dosage Form : Injectable; Injection
Dosage Strength : 50MG/VIAL
Packaging :
Approval Date :
Application Number : 89307
Regulatory Info :
Registration Country : USA