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    Approved Drug Products containing 18723 listed in the FDA Orange Book. Original Data : FDA Website

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    Bora Pharmaceuticals- Making success more certain.

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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications.

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    Axplora- The partner of choice for complex APIs.

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    Fareva is a one-stop-shop for API/HPAPI, OSD & Sterile products, is USFDA, EMA and PMDA-inspected and has multiple NDA & ANDA filings.

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    AbbVie Inc

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    Brand Name : DEPAKOTE

    U.S.A
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    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 500MG VALPROIC ACID

    Approval Date : 1983-03-10

    Application Number : 18723

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    02

    Brand Name : DEPAKOTE

    U.S.A
    Luxepack
    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 125MG VALPROIC ACID

    Approval Date : 1984-10-26

    Application Number : 18723

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    03

    Brand Name : DEPAKOTE

    U.S.A
    Luxepack
    Not Confirmed
    arrow
    • 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.
    Contact Supplier Contact Supplier
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    Abbvie Company Banner

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
    Place