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    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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    Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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    Appco Pharmaceutical Corp

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    01 2ACETAZOLAMIDE

    02 2AMINOCAPROIC ACID

    03 2BACLOFEN

    04 3BUMETANIDE

    05 5CHLORPROMAZINE HYDROCHLORIDE

    06 2CHLORTHALIDONE

    07 1CYPROHEPTADINE HYDROCHLORIDE

    08 5DOXEPIN HYDROCHLORIDE

    09 4HYDROXYCHLOROQUINE SULFATE

    10 4LABETALOL HYDROCHLORIDE

    11 2MODAFINIL

    12 4PERPHENAZINE

    13 3PRAZOSIN HYDROCHLORIDE

    14 2RANITIDINE HYDROCHLORIDE

    15 3SERTRALINE HYDROCHLORIDE

    16 3SILDENAFIL CITRATE

    17 1VALGANCICLOVIR HYDROCHLORIDE

    18 2VENLAFAXINE HYDROCHLORIDE

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    01

    Brand Name : ACETAZOLAMIDE

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : ACETAZOLAMIDE

    U.S.A
    Pharmtech & Ingredients
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    RLD : No

    TE Code : AB

    ACETAZOLAMIDE

    Appco Pharmaceutical Corp

    Dosage Form : TABLET; ORAL

    Proprietary Name : ACETAZOLAMIDE

    Dosage Strength : 125MG

    Approval Date : 2021-02-22

    Application Number : 211372

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    02

    Brand Name : ACETAZOLAMIDE

    U.S.A
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    Brand Name : ACETAZOLAMIDE

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    RLD : No

    TE Code : AB

    ACETAZOLAMIDE

    Appco Pharmaceutical Corp

    Dosage Form : TABLET; ORAL

    Proprietary Name : ACETAZOLAMIDE

    Dosage Strength : 250MG

    Approval Date : 2021-02-22

    Application Number : 211372

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    Brand Name : AMINOCAPROIC ACID

    U.S.A
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    Brand Name : AMINOCAPROIC ACID

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    RLD : No

    TE Code : AB

    AMINOCAPROIC ACID

    Appco Pharmaceutical Corp

    Dosage Form : TABLET; ORAL

    Proprietary Name : AMINOCAPROIC ACID

    Dosage Strength : 500MG

    Approval Date : 2022-09-14

    Application Number : 213944

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Brand Name : AMINOCAPROIC ACID

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    Brand Name : AMINOCAPROIC ACID

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    RLD : No

    TE Code : AB

    AMINOCAPROIC ACID

    Appco Pharmaceutical Corp

    Dosage Form : TABLET; ORAL

    Proprietary Name : AMINOCAPROIC ACID

    Dosage Strength : 1GM

    Approval Date : 2022-09-14

    Application Number : 213944

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    Brand Name : BACLOFEN

    U.S.A
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    Brand Name : BACLOFEN

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    RLD : No

    TE Code :

    BACLOFEN

    Appco Pharmaceutical Corp

    Dosage Form : TABLET; ORAL

    Proprietary Name : BACLOFEN

    Dosage Strength : 10MG

    Approval Date : 2010-02-18

    Application Number : 90334

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    Brand Name : BACLOFEN

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : BACLOFEN

    U.S.A
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    RLD : No

    TE Code :

    BACLOFEN

    Appco Pharmaceutical Corp

    Dosage Form : TABLET; ORAL

    Proprietary Name : BACLOFEN

    Dosage Strength : 20MG

    Approval Date : 2010-02-18

    Application Number : 90334

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    Brand Name : BUMETANIDE

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : BUMETANIDE

    U.S.A
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    RLD : No

    TE Code : AB

    BUMETANIDE

    Appco Pharmaceutical Corp

    Dosage Form : TABLET; ORAL

    Proprietary Name : BUMETANIDE

    Dosage Strength : 0.5MG

    Approval Date : 2024-09-18

    Application Number : 212931

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    08

    Brand Name : BUMETANIDE

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : BUMETANIDE

    U.S.A
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    RLD : No

    TE Code : AB

    BUMETANIDE

    Appco Pharmaceutical Corp

    Dosage Form : TABLET; ORAL

    Proprietary Name : BUMETANIDE

    Dosage Strength : 1MG

    Approval Date : 2024-09-18

    Application Number : 212931

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    09

    Brand Name : BUMETANIDE

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : BUMETANIDE

    U.S.A
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    RLD : No

    TE Code : AB

    BUMETANIDE

    Appco Pharmaceutical Corp

    Dosage Form : TABLET; ORAL

    Proprietary Name : BUMETANIDE

    Dosage Strength : 2MG

    Approval Date : 2024-09-18

    Application Number : 212931

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    10

    Brand Name : CHLORPROMAZINE HYDRO...

    U.S.A
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    Not Confirmed
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    Brand Name : CHLORPROMAZINE HYDRO...

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    • fda
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    RLD : No

    TE Code : AB

    CHLORPROMAZINE HYDROCHLORIDE

    Appco Pharmaceutical Corp

    Dosage Form : TABLET; ORAL

    Proprietary Name : CHLORPROMAZINE HYDROCHLO...

    Dosage Strength : 10MG

    Approval Date : 2020-08-31

    Application Number : 213590

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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