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    Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.

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    Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.

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    IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.

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    Cosma S.p.A., part of CFM Group with AMSA & Clarochem, provides global pharma & veterinary health with 300+ tons of FDA-approved APIs.

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    Sodium Nitroprusside

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    01 1AbbVie Inc

    02 1Biophore India Pharmaceuticals Pvt Ltd

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    07 1Adcock Ingram

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    16 1Chartwell Pharmaceuticals llc

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    41 1Teva Pharmaceutical Industries

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    AbbVie Inc

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    SODIUM NITROPRUSSIDE

    Brand Name : NITROPRESS

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1982-01-01

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    Biophore India Pharmaceuticals Pvt ...

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    Virtual BoothBiophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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    Dr. Reddy's Laboratories

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    SODIUM NITROPRUSSIDE

    Brand Name : SODIUM NITROPRUSSIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 25MG/ML

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    Approval Date : 2019-04-10

    Application Number : 210114

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    Abbott Laboratories

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    Brand Name : NITROPRESS

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    Approval Date : 1987-11-16

    Application Number : 71555

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    ABRAXIS PHARM

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    Approval Date : 1985-01-17

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    Amneal Pharmaceuticals

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    Approval Date : 2017-11-07

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    Avet Pharmaceuticals

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    Brand Name : SODIUM NITROPRUSSIDE

    Dosage Form : INJECTABLE;INJECTION

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    Approval Date : 2022-11-08

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    Bausch Health

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    Approval Date : 1988-08-01

    Application Number : 71961

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    Baxter Healthcare Corporation

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    SODIUM NITROPRUSSIDE

    Brand Name : SODIUM NITROPRUSSIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1982-07-28

    Application Number : 18581

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    Epic Pharma. LLC.

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    Dosage Form : INJECTABLE;INJECTION

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    Approval Date : 2017-05-04

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    Exela Pharma Sciences, LLC.

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    SODIUM NITROPRUSSIDE

    Brand Name : NIPRIDE RTU IN SODIUM CHLORIDE 0.9%

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 50MG/100ML (0.5MG/ML)

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    Approval Date : 2017-03-08

    Application Number : 209387

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    Exela Pharma Sciences, LLC.

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    Brand Name : NIPRIDE RTU IN SODIUM CHLORIDE 0.9%

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 10MG/50ML (0.2MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2017-12-07

    Application Number : 209387

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    Exela Pharma Sciences, LLC.

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    SODIUM NITROPRUSSIDE

    Brand Name : NIPRIDE RTU IN SODIUM CHLORIDE 0.9%

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 20MG/100ML (0.2MG/ML)

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    Approval Date : 2018-07-13

    Application Number : 209387

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    F. Hoffmann-La Roche

    Switzerland
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    Brand Name : NIPRIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/VIAL

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    Approval Date : 1982-01-01

    Application Number : 17546

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    Registration Country : USA

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    Hospira, Inc.

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    Dosage Strength : 50MG/VIAL

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    Approval Date : 1986-06-09

    Application Number : 70566

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    Micro Labs Limited

    India
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    Dosage Strength : 25MG/ML

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    Approval Date : 2017-12-08

    Application Number : 209352

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    Nexus Pharmaceuticals

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    Approval Date : 2017-05-25

    Application Number : 207499

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    Sagent Pharmaceuticals

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    Brand Name : SODIUM NITROPRUSSIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 25MG/ML

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    Approval Date : 2016-12-08

    Application Number : 207426

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    Teva Pharmaceutical Industries

    Israel
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    Dosage Strength : 25MG/ML

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    Approval Date : 1992-03-30

    Application Number : 73465

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    Registration Country : USA

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    PHARMOBEDIENT

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    Approval Date : 2018-08-10

    Application Number : 209584

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