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    European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

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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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    USP reference standards; highly characterized specimens of drug substances, impurities, excipients, degradation products & more.

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    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.

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    Guizhou Utide Biotechnology Co., Ltd. - Specialized GMP manufacturing for next-generation GLP-1 peptide APIs.

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    Sodium Nitroprusside

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    AbbVie Inc

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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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    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    Dosage Strength : 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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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    Exela Pharma Sciences, LLC.

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    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

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

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    Approval Date : 2018-07-13

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    F. Hoffmann-La Roche

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    Brand Name : NIPRIDE

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    Approval Date : 1982-01-01

    Application Number : 17546

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    Hospira, Inc.

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    Approval Date : 1986-06-09

    Application Number : 70566

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    Micro Labs Limited

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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

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    Sagent Pharmaceuticals

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    Approval Date : 2016-12-08

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    Teva Pharmaceutical Industries

    Israel
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    Approval Date : 1992-03-30

    Application Number : 73465

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