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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    End-to-end drug development, specializing in high-potency softgels and liquids, providing global partners with a competitive advantage.

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    Kewpie is your partner for Sodium Hyaluronate & Hyaluronic Acid// CEP, USDMF, KDMF & JDMF registered.

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    01 3Mankind Pharma

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    04 3Amneal Pharmaceuticals

    05 3Appco Pharmaceutical Corp

    06 1Aspiro Pharma

    07 3Avet Pharmaceuticals

    08 1Corstasis Therapeutics

    09 1Ebb Medical

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    11 1GLAND PHARMA LIMITED

    12 2Hospira, Inc.

    13 3Jubilant Generics

    14 12Karo Pharma

    15 1Lupin Ltd

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    18 2NM Pharma Limited

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    25 3Rising Pharmaceuticals Inc

    26 3Rubicon Research

    27 1Sagent Pharmaceuticals

    28 3Sandoz B2B

    29 3Taro Pharmaceutical Industries

    30 1Teva Pharmaceutical Industries

    31 3Upsher-Smith Laboratories

    32 4VALIDUS PHARMS

    33 1Viatris

    34 1West-ward Pharmaceutical Corp

    35 3Zydus Pharmaceuticals

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    Mankind Pharma

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    Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

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    BUMETANIDE

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    Approval Date : 2025-04-03

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    Mankind Pharma

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    Approval Date : 2025-04-03

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    Mankind Pharma

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    Approval Date : 2025-04-03

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    Avet Pharmaceuticals

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    BUMETANIDE

    Brand Name : BUMETANIDE

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    Approval Date : 1995-04-24

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    Avet Pharmaceuticals

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    Approval Date : 1995-04-24

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    Avet Pharmaceuticals

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    BUMETANIDE

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    Approval Date : 1995-04-24

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    Hospira, Inc.

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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : INJECTABLE;INJECTION

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    Approval Date : 1997-10-30

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    Hospira, Inc.

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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : INJECTABLE;INJECTION

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    Approval Date : 1994-10-31

    Application Number : 74332

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    Sagent Pharmaceuticals

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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : INJECTABLE;INJECTION

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    Approval Date : 1995-01-27

    Application Number : 74441

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    Sandoz B2B

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    BUMETANIDE

    Brand Name : BUMETANIDE

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    Approval Date : 1996-11-21

    Application Number : 74700

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    Sandoz B2B

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    Approval Date : 1996-11-21

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    Sandoz B2B

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    BUMETANIDE

    Brand Name : BUMETANIDE

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    Approval Date : 1996-11-21

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    Teva Pharmaceutical Industries

    Israel
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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.25MG/ML

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    Approval Date : 1997-11-18

    Application Number : 74613

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    VALIDUS PHARMS

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    BUMETANIDE

    Brand Name : BUMEX

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG

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    Approval Date : 1983-02-28

    Application Number : 18225

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    Registration Country : USA

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    VALIDUS PHARMS

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    Brand Name : BUMEX

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    Approval Date : 1983-02-28

    Application Number : 18225

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    VALIDUS PHARMS

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    Brand Name : BUMEX

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    Dosage Strength : 2MG

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    Approval Date : 1985-06-14

    Application Number : 18225

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    Registration Country : USA

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    VALIDUS PHARMS

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    BUMETANIDE

    Brand Name : BUMEX

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1983-02-28

    Application Number : 18226

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    West-ward Pharmaceutical Corp

    U.S.A
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    West-ward Pharmaceutical Corp

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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.25MG/ML

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    Approval Date : 2008-04-30

    Application Number : 79196

    Regulatory Info : RX

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    Zydus Pharmaceuticals

    U.S.A
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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.5MG

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    Approval Date : 2018-04-30

    Application Number : 202900

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    Registration Country : USA

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    Zydus Pharmaceuticals

    U.S.A
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    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

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    Approval Date : 2018-04-30

    Application Number : 202900

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