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    Approved Drug Products of Appco Pharmaceutical Corp listed in the FDA Orange Book. Original Data : FDA Website

    Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

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    Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.

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    xyz-pharma-m-2024-09-09

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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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    LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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    xyz-pharma-m-2024-09-09

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    Appco Pharmaceutical Corp

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    01 2ACETAZOLAMIDE

    02 2BACLOFEN

    03 3BUMETANIDE

    04 5CHLORPROMAZINE HYDROCHLORIDE

    05 2CHLORTHALIDONE

    06 1CYPROHEPTADINE HYDROCHLORIDE

    07 5DOXEPIN HYDROCHLORIDE

    08 4DOXYCYCLINE

    09 4HYDROXYCHLOROQUINE SULFATE

    10 3LABETALOL HYDROCHLORIDE

    11 1METAXALONE

    12 2MODAFINIL

    13 4PERPHENAZINE

    14 3PRAZOSIN HYDROCHLORIDE

    15 2RANITIDINE HYDROCHLORIDE

    16 3SERTRALINE HYDROCHLORIDE

    17 4SILDENAFIL CITRATE

    18 2TIZANIDINE HYDROCHLORIDE

    19 1VALGANCICLOVIR HYDROCHLORIDE

    20 2VENLAFAXINE HYDROCHLORIDE

    21 2ZOLMITRIPTAN

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    01

    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 : 125MG

    Approval Date : 2021-02-22

    Application Number : 211372

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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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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    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

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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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    Brand Name : BUMETANIDE

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    TE Code :

    BUMETANIDE

    Appco Pharmaceutical Corp

    Dosage Form : TABLET; ORAL

    Proprietary Name : BUMETANIDE

    Dosage Strength : 0.5MG

    Approval Date :

    Application Number : 212931

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    TE Code :

    BUMETANIDE

    Appco Pharmaceutical Corp

    Dosage Form : TABLET; ORAL

    Proprietary Name : BUMETANIDE

    Dosage Strength : 1MG

    Approval Date :

    Application Number : 212931

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    TE Code :

    BUMETANIDE

    Appco Pharmaceutical Corp

    Dosage Form : TABLET; ORAL

    Proprietary Name : BUMETANIDE

    Dosage Strength : 2MG

    Approval Date :

    Application Number : 212931

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    Brand Name : CHLORPROMAZINE HYDRO...

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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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    RLD : No

    TE Code : AB

    CHLORPROMAZINE HYDROCHLORIDE

    Appco Pharmaceutical Corp

    Dosage Form : TABLET; ORAL

    Proprietary Name : CHLORPROMAZINE HYDROCHLO...

    Dosage Strength : 25MG

    Approval Date : 2020-08-31

    Application Number : 213590

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    RLD : No

    TE Code : AB

    CHLORPROMAZINE HYDROCHLORIDE

    Appco Pharmaceutical Corp

    Dosage Form : TABLET; ORAL

    Proprietary Name : CHLORPROMAZINE HYDROCHLO...

    Dosage Strength : 50MG

    Approval Date : 2020-08-31

    Application Number : 213590

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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