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    Trusted Global CDMO Partner Delivering End-to-End Pharma Manufacturing & Development Solutions.

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    Evonik Health Care is the innovation hub for leading life science companies

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    Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.

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    Axplora is your partner of choice for complex APIs.

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    Munit offers scalable GMP micronization and particle size engineering to enhance drug solubility, bioavailability, and performance.

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    Brand Name : DIVALPROEX SODIUM

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    Brand Name : DIVALPROEX SODIUM

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    RLD : No

    TE Code : AB

    DIVALPROEX SODIUM

    Upsher-Smith Laboratories

    Dosage Form : TABLET, DELAYED RELEASE; ORAL

    Proprietary Name : DIVALPROEX SODIUM

    Dosage Strength : EQ 125MG VALPROIC ACID

    Approval Date : 2008-07-29

    Application Number : 78182

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Brand Name : DIVALPROEX SODIUM

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    BePharma
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    Brand Name : DIVALPROEX SODIUM

    U.S.A
    BePharma
    Not Confirmed
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    • WHO-GMP
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    RLD : No

    TE Code : AB

    DIVALPROEX SODIUM

    Upsher-Smith Laboratories

    Dosage Form : TABLET, DELAYED RELEASE; ORAL

    Proprietary Name : DIVALPROEX SODIUM

    Dosage Strength : EQ 250MG VALPROIC ACID

    Approval Date : 2008-07-29

    Application Number : 78182

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Brand Name : DIVALPROEX SODIUM

    U.S.A
    BePharma
    Not Confirmed
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    Brand Name : DIVALPROEX SODIUM

    U.S.A
    BePharma
    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.
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    RLD : No

    TE Code : AB

    DIVALPROEX SODIUM

    Upsher-Smith Laboratories

    Dosage Form : TABLET, DELAYED RELEASE; ORAL

    Proprietary Name : DIVALPROEX SODIUM

    Dosage Strength : EQ 500MG VALPROIC ACID

    Approval Date : 2008-07-29

    Application Number : 78182

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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