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    04 3Amneal Pharmaceuticals

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    06 3Appco Pharmaceutical Corp

    07 1Aspiro Pharma

    08 3Avet Pharmaceuticals

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    12 1GLAND PHARMA LIMITED

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    17 4MSN Laboratories

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    20 2NM Pharma Limited

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    22 1Nordic Prime Aps

    23 15ORIFARM GROUP AS

    24 2P & D Pharmaceuticals Limited

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    26 2Pharma Regulatory Services Limited

    27 1Qilu Pharmaceutical

    28 1Remedica Limited

    29 3Rising Pharmaceuticals Inc

    30 3Rubicon Research

    31 1Sagent Pharmaceuticals

    32 3Sandoz B2B

    33 3Taro Pharmaceutical Industries

    34 1Teva Pharmaceutical Industries

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    01

    Mankind Pharma

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    Approval Date : 2025-04-03

    Application Number : 219291

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    Mankind Pharma

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    Approval Date : 2025-04-03

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    03

    Mankind Pharma

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    BUMETANIDE

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    Approval Date : 2025-04-03

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    04

    Avet Pharmaceuticals

    U.S.A
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    BUMETANIDE

    Brand Name : BUMETANIDE

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    Approval Date : 1995-04-24

    Application Number : 74225

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    05

    Avet Pharmaceuticals

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    Approval Date : 1995-04-24

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    06

    Avet Pharmaceuticals

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    BUMETANIDE

    Brand Name : BUMETANIDE

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    Approval Date : 1995-04-24

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    07

    Hospira, Inc.

    U.S.A
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    Regulatory Info : DISCN

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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : INJECTABLE;INJECTION

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    Approval Date : 1997-10-30

    Application Number : 74160

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    Hospira, Inc.

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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.25MG/ML

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    Approval Date : 1994-10-31

    Application Number : 74332

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    09

    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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    10

    Sandoz B2B

    Switzerland
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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

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    Approval Date : 1996-11-21

    Application Number : 74700

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    11

    Sandoz B2B

    Switzerland
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    Sandoz B2B

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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

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    Approval Date : 1996-11-21

    Application Number : 74700

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    12

    Sandoz B2B

    Switzerland
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    Sandoz B2B

    Switzerland
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    Nutri Ingredients Summit
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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

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    Approval Date : 1996-11-21

    Application Number : 74700

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    13

    Teva Pharmaceutical Industries

    Israel
    Nutri Ingredients Summit
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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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    14

    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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    15

    VALIDUS PHARMS

    U.S.A
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    VALIDUS PHARMS

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    Nutri Ingredients Summit
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    BUMETANIDE

    Brand Name : BUMEX

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.5MG

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    Approval Date : 1983-02-28

    Application Number : 18225

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    Registration Country : USA

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    16

    VALIDUS PHARMS

    U.S.A
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    VALIDUS PHARMS

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    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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    VALIDUS PHARMS

    U.S.A
    Nutri Ingredients Summit
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    VALIDUS PHARMS

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    Regulatory Info : DISCN

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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

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    West-ward Pharmaceutical Corp

    U.S.A
    Nutri Ingredients Summit
    Not Confirmed
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    West-ward Pharmaceutical Corp

    U.S.A
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    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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    Zydus Pharmaceuticals

    U.S.A
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    Zydus Pharmaceuticals

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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 : 2018-04-30

    Application Number : 202900

    Regulatory Info : RX

    Registration Country : USA

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    Zydus Pharmaceuticals

    U.S.A
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    BUMETANIDE

    Brand Name : BUMETANIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG

    Packaging :

    Approval Date : 2018-04-30

    Application Number : 202900

    Regulatory Info : RX

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.