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    Approval Date : 1982-10-20

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    Avet Pharmaceuticals

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    ACETAZOLAMIDE

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    Approval Date : 2008-12-10

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    Avet Pharmaceuticals

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    Approval Date : 1985-10-22

    Application Number : 88882

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    Approval Date : 2016-10-27

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    Cadila Pharmaceuticals

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    Approval Date : 2019-01-16

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    Approval Date : 1982-02-05

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    Approval Date : 2011-07-14

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    Approval Date : 2020-10-01

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    Approval Date : 2016-03-29

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    Novast Laboratories

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    Approval Date : 2016-09-30

    Application Number : 203434

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    Rising Pharmaceuticals Inc

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    Brand Name : ACETAZOLAMIDE

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    Approval Date : 2019-06-18

    Application Number : 203917

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    Sun Pharmaceutical Industries Limit...

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    Brand Name : ACETAZOLAMIDE

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    Approval Date : 1988-06-22

    Application Number : 89753

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    Regulatory Info : DISCN

    Registration Country : USA

    ACETAZOLAMIDE

    Brand Name : ACETAZOLAMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 125MG

    Packaging :

    Approval Date : 1988-06-22

    Application Number : 89753

    Regulatory Info : DISCN

    Registration Country : USA

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    Regulatory Info : RX

    Registration Country : USA

    ACETAZOLAMIDE

    Brand Name : ACETAZOLAMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 125MG

    Packaging :

    Approval Date : 1997-05-28

    Application Number : 40195

    Regulatory Info : RX

    Registration Country : USA

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    Regulatory Info : RX

    Registration Country : USA

    ACETAZOLAMIDE

    Brand Name : ACETAZOLAMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 250MG

    Packaging :

    Approval Date : 1997-05-28

    Application Number : 40195

    Regulatory Info : RX

    Registration Country : USA

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    28

    Teva Pharmaceutical Industries

    Israel
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    Regulatory Info : DISCN

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    ACETAZOLAMIDE

    Brand Name : DIAMOX

    Dosage Form : TABLET;ORAL

    Dosage Strength : 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 8943

    Regulatory Info : DISCN

    Registration Country : USA

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    Regulatory Info : DISCN

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    ACETAZOLAMIDE

    Brand Name : DIAMOX

    Dosage Form : TABLET;ORAL

    Dosage Strength : 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 8943

    Regulatory Info : DISCN

    Registration Country : USA

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    30

    Teva Pharmaceutical Industries

    Israel
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    Israel
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    Regulatory Info : DISCN

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    ACETAZOLAMIDE

    Brand Name : DIAMOX

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 12945

    Regulatory Info : DISCN

    Registration Country : USA

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