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    Sharp is a global leader in pharmaceutical packaging and clinical trial supply services.

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    Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.

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

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    Bumex, Bumetanide

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    01

    Mankind Pharma

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    BUMETANIDE

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    Approval Date : 2025-04-03

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    Mankind Pharma

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    Mankind Pharma

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    04

    Amneal Pharmaceuticals

    U.S.A
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    BUMETANIDE

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    Approval Date : 2017-10-18

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    05

    Amneal Pharmaceuticals

    U.S.A
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    Approval Date : 2017-10-18

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    06

    Amneal Pharmaceuticals

    U.S.A
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    Approval Date : 2017-10-18

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    07

    Avet Pharmaceuticals

    U.S.A
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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

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    Approval Date : 1995-04-24

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    08

    Avet Pharmaceuticals

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    Approval Date : 1995-04-24

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    09

    Avet Pharmaceuticals

    U.S.A
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    Brand Name : BUMETANIDE

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    Approval Date : 1995-04-24

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    10

    Hospira, Inc.

    U.S.A
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    AACR Annual meeting
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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.25MG/ML

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    Approval Date : 1997-10-30

    Application Number : 74160

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    11

    Hospira, Inc.

    U.S.A
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    Hospira, Inc.

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    AACR Annual meeting
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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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    12

    Rising Pharmaceuticals Inc

    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 : 2019-12-12

    Application Number : 212019

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    Registration Country : USA

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    13

    Rising Pharmaceuticals Inc

    U.S.A
    AACR Annual meeting
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    Rising Pharmaceuticals Inc

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    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG

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    Approval Date : 2019-12-12

    Application Number : 212019

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    14

    Rising Pharmaceuticals Inc

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Rising Pharmaceuticals Inc

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    AACR Annual meeting
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    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2MG

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    Approval Date : 2019-12-12

    Application Number : 212019

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    15

    Sagent Pharmaceuticals

    U.S.A
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    Sagent Pharmaceuticals

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    AACR Annual meeting
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    Brand Name : BUMETANIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.25MG/ML

    Packaging :

    Approval Date : 1995-01-27

    Application Number : 74441

    Regulatory Info : RX

    Registration Country : USA

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    16

    Sandoz B2B

    Switzerland
    AACR Annual meeting
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    Switzerland
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    AACR Annual meeting
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    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.5MG

    Packaging :

    Approval Date : 1996-11-21

    Application Number : 74700

    Regulatory Info : RX

    Registration Country : USA

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    17

    Sandoz B2B

    Switzerland
    AACR Annual meeting
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    Switzerland
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    AACR Annual meeting
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    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG

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    Approval Date : 1996-11-21

    Application Number : 74700

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    18

    Sandoz B2B

    Switzerland
    AACR Annual meeting
    Not Confirmed
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    Sandoz B2B

    Switzerland
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    AACR Annual meeting
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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2MG

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    Approval Date : 1996-11-21

    Application Number : 74700

    Regulatory Info : RX

    Registration Country : USA

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    19

    Teva Pharmaceutical Industries

    Israel
    AACR Annual meeting
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    Regulatory Info : DISCN

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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.25MG/ML

    Packaging :

    Approval Date : 1997-11-18

    Application Number : 74613

    Regulatory Info : DISCN

    Registration Country : USA

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    Upsher-Smith Laboratories

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    U.S.A
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    Regulatory Info : RX

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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.5MG

    Packaging :

    Approval Date : 2018-01-23

    Application Number : 209916

    Regulatory Info : RX

    Registration Country : USA

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    21

    Upsher-Smith Laboratories

    U.S.A
    AACR Annual meeting
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    U.S.A
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    AACR Annual meeting
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    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG

    Packaging :

    Approval Date : 2018-01-23

    Application Number : 209916

    Regulatory Info : RX

    Registration Country : USA

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    22

    Upsher-Smith Laboratories

    U.S.A
    AACR Annual meeting
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    U.S.A
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    AACR Annual meeting
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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2MG

    Packaging :

    Approval Date : 2018-01-23

    Application Number : 209916

    Regulatory Info : RX

    Registration Country : USA

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    23

    VALIDUS PHARMS

    U.S.A
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    VALIDUS PHARMS

    U.S.A
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    Regulatory Info : RX

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    BUMETANIDE

    Brand Name : BUMEX

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG

    Packaging :

    Approval Date : 1983-02-28

    Application Number : 18225

    Regulatory Info : RX

    Registration Country : USA

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    VALIDUS PHARMS

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    VALIDUS PHARMS

    U.S.A
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    AACR Annual meeting
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    Regulatory Info : RX

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    BUMETANIDE

    Brand Name : BUMEX

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.5MG

    Packaging :

    Approval Date : 1983-02-28

    Application Number : 18225

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    VALIDUS PHARMS

    U.S.A
    AACR Annual meeting
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    VALIDUS PHARMS

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    BUMETANIDE

    Brand Name : BUMEX

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2MG

    Packaging :

    Approval Date : 1985-06-14

    Application Number : 18225

    Regulatory Info : RX

    Registration Country : USA

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    26

    VALIDUS PHARMS

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    VALIDUS PHARMS

    U.S.A
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    AACR Annual meeting
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 1983-02-28

    Application Number : 18226

    Regulatory Info : DISCN

    Registration Country : USA

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    27

    West-ward Pharmaceutical Corp

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    West-ward Pharmaceutical Corp

    U.S.A
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    AACR Annual meeting
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : RX

    Registration Country : USA

    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.25MG/ML

    Packaging :

    Approval Date : 2008-04-30

    Application Number : 79196

    Regulatory Info : RX

    Registration Country : USA

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    28

    Zydus Pharmaceuticals

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Zydus Pharmaceuticals

    U.S.A
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    AACR Annual meeting
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : RX

    Registration Country : USA

    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.5MG

    Packaging :

    Approval Date : 2018-04-30

    Application Number : 202900

    Regulatory Info : RX

    Registration Country : USA

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    29

    Zydus Pharmaceuticals

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Zydus Pharmaceuticals

    U.S.A
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    AACR Annual meeting
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : RX

    Registration Country : USA

    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG

    Packaging :

    Approval Date : 2018-04-30

    Application Number : 202900

    Regulatory Info : RX

    Registration Country : USA

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    30

    Zydus Pharmaceuticals

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Zydus Pharmaceuticals

    U.S.A
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    AACR Annual meeting
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : RX

    Registration Country : USA

    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2MG

    Packaging :

    Approval Date : 2018-04-30

    Application Number : 202900

    Regulatory Info : RX

    Registration Country : USA

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