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    Brinzolamide

    ACTIVE PHARMA INGREDIENTS

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    01 1ALCON LABS INC

    02 1BAUSCH AND LOMB

    03 1PADAGIS US

    04 1SANDOZ

    05 1WATSON LABS INC

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    01

    WATSON LABS INC

    Ireland
    Fi Europe 2024
    Not Confirmed
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    WATSON LABS INC

    Ireland
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    Fi Europe 2024
    Not Confirmed
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    RLD : No

    TE Code : AB

    BRINZOLAMIDE

    Brand Name : BRINZOLAMIDE

    Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

    Dosage Strength : 1%

    Approval Date : 2020-11-27

    Application Number : 209406

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    02

    ALCON LABS INC

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    ALCON LABS INC

    U.S.A
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    Fi Europe 2024
    Not Confirmed
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    RLD : Yes

    TE Code :

    BRIMONIDINE TARTRATE; BRINZOLAMIDE

    Brand Name : SIMBRINZA

    Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

    Dosage Strength : 0.2%;1%

    Approval Date : 2013-04-19

    Application Number : 204251

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    03

    BAUSCH AND LOMB

    Canada
    Fi Europe 2024
    Not Confirmed
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    BAUSCH AND LOMB

    Canada
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    RLD : No

    TE Code : AB

    BRINZOLAMIDE

    Brand Name : BRINZOLAMIDE

    Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

    Dosage Strength : 1%

    Approval Date : 2021-08-18

    Application Number : 204884

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    04

    PADAGIS US

    Israel
    Fi Europe 2024
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    PADAGIS US

    Israel
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    Fi Europe 2024
    Not Confirmed
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    RLD : No

    TE Code : AB

    BRINZOLAMIDE

    Brand Name : BRINZOLAMIDE

    Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

    Dosage Strength : 1%

    Approval Date : 2023-07-28

    Application Number : 211914

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    SANDOZ

    Switzerland
    Fi Europe 2024
    Not Confirmed
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    SANDOZ

    Switzerland
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    Fi Europe 2024
    Not Confirmed
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    RLD : Yes

    TE Code : AB

    BRINZOLAMIDE

    Brand Name : AZOPT

    Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

    Dosage Strength : 1%

    Approval Date : 1998-04-01

    Application Number : 20816

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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