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    AbbVie Inc

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    Brand Name : DEPAKOTE

    U.S.A
    AAPS
    Not Confirmed
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    RLD : Yes

    TE Code : AB

    DIVALPROEX SODIUM

    AbbVie Inc

    Dosage Form : TABLET, DELAYED RELEASE; ORAL

    Proprietary Name : DEPAKOTE

    Dosage Strength : EQ 125MG VALPROIC ACID

    Approval Date : 1984-10-26

    Application Number : 18723

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    02

    Brand Name : DEPAKOTE

    U.S.A
    AAPS
    Not Confirmed
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    • fda
    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code : AB

    DIVALPROEX SODIUM

    AbbVie Inc

    Dosage Form : TABLET, DELAYED RELEASE; ORAL

    Proprietary Name : DEPAKOTE

    Dosage Strength : EQ 250MG VALPROIC ACID

    Approval Date : 1983-03-10

    Application Number : 18723

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    03

    Brand Name : DEPAKOTE

    U.S.A
    AAPS
    Not Confirmed
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    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    RLD : Yes

    TE Code : AB

    DIVALPROEX SODIUM

    AbbVie Inc

    Dosage Form : TABLET, DELAYED RELEASE; ORAL

    Proprietary Name : DEPAKOTE

    Dosage Strength : EQ 500MG VALPROIC ACID

    Approval Date : 1983-03-10

    Application Number : 18723

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

    Abbvie Company Banner

    Product
    Web Link

    Stock Recap
    #PipelineProspector

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