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    Approved Drug Products containing 200920 listed in the FDA Orange Book. Original Data : FDA Website

    Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

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    Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.

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    xyz-pharma-m-2024-09-09

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    Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.

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    LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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    xyz-pharma-m-2024-09-09

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    Actavis Inc

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    01 2ACTAVIS ELIZABETH

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    Brand Name : FENOFIBRIC ACID

    Ireland
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    Brand Name : FENOFIBRIC ACID

    Ireland
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    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

    CHOLINE FENOFIBRATE

    Actavis Inc

    Dosage Form : CAPSULE, DELAYED RELEASE; ORAL

    Proprietary Name : FENOFIBRIC ACID

    Dosage Strength : EQ 135MG FENOFIBRIC ACID

    Approval Date : 2015-10-07

    Application Number : 200920

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Brand Name : FENOFIBRIC ACID

    Ireland
    Formnext Forum
    Not Confirmed
    arrow

    Brand Name : FENOFIBRIC ACID

    Ireland
    Formnext Forum
    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 Ireland
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : No

    TE Code : AB

    CHOLINE FENOFIBRATE

    Actavis Inc

    Dosage Form : CAPSULE, DELAYED RELEASE; ORAL

    Proprietary Name : FENOFIBRIC ACID

    Dosage Strength : EQ 45MG FENOFIBRIC ACID

    Approval Date : 2015-10-07

    Application Number : 200920

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Stock Recap
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