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    Approved Drug Products containing 213137 listed in the FDA Orange Book. Original Data : FDA Website

    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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    FAMAR CDMO- From early development to commercial manufacturing.

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    xyz-pharma-m-2024-09-09

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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.

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    Veranova: A CDMO that manages complexity with confidence.

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    xyz-pharma-m-2024-09-09

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    Global Blood Therapeutics

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    01 2GLOBAL BLOOD THERAPS

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    01

    Brand Name : OXBRYTA

    U.S.A
    BioProcess International
    Not Confirmed
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    Brand Name : OXBRYTA

    U.S.A
    BioProcess International
    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 : Yes

    TE Code :

    VOXELOTOR

    Global Blood Therapeutics

    Dosage Form : TABLET; ORAL

    Proprietary Name : OXBRYTA

    Dosage Strength : 500MG

    Approval Date : 2019-11-25

    Application Number : 213137

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    02

    Brand Name : OXBRYTA

    U.S.A
    BioProcess International
    Not Confirmed
    arrow

    Brand Name : OXBRYTA

    U.S.A
    BioProcess International
    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 : Yes

    TE Code :

    VOXELOTOR

    Global Blood Therapeutics

    Dosage Form : TABLET; ORAL

    Proprietary Name : OXBRYTA

    Dosage Strength : 300MG

    Approval Date : 2022-10-14

    Application Number : 213137

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

    blank

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
    Place