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    Approved Drug Products containing 217732 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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    Creekwood Pharmaceuticals

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    Brand Name : FENOFIBRATE

    U.S.A
    Discovery on Target
    Not Confirmed
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    Brand Name : FENOFIBRATE

    U.S.A
    Discovery on Target
    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 : No

    TE Code : BX

    FENOFIBRATE

    Creekwood Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : FENOFIBRATE

    Dosage Strength : 120MG

    Approval Date : 2023-09-07

    Application Number : 217732

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : BX

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    02

    Brand Name : FENOFIBRATE

    U.S.A
    Discovery on Target
    Not Confirmed
    arrow

    Brand Name : FENOFIBRATE

    U.S.A
    Discovery on Target
    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 U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : No

    TE Code : BX

    FENOFIBRATE

    Creekwood Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : FENOFIBRATE

    Dosage Strength : 40MG

    Approval Date : 2023-09-07

    Application Number : 217732

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : BX

    blank

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
    Place