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    Approved Drug Products containing 209286 listed in the FDA Orange Book. Original Data : FDA Website

    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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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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    Lupin Ltd

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    Brand Name : DIVALPROEX SODIUM

    India
    Luxepack
    Not Confirmed
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    Brand Name : DIVALPROEX SODIUM

    India
    Luxepack
    Not Confirmed
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    • 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

    Lupin Ltd

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : DIVALPROEX SODIUM

    Dosage Strength : EQ 500MG VALPROIC ACID

    Approval Date : 2019-10-18

    Application Number : 209286

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Brand Name : DIVALPROEX SODIUM

    India
    Luxepack
    Not Confirmed
    arrow

    Brand Name : DIVALPROEX SODIUM

    India
    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.
    Post an Enquiry Post an Enquiry
    Flag India
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : No

    TE Code : AB

    DIVALPROEX SODIUM

    Lupin Ltd

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : DIVALPROEX SODIUM

    Dosage Strength : EQ 250MG VALPROIC ACID

    Approval Date : 2019-10-18

    Application Number : 209286

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Product
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    Stock Recap
    #PipelineProspector

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