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    Approved Drug Products containing 213176 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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    Brand Name : UKONIQ

    U.S.A
    FNCE 2024
    Not Confirmed
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    Brand Name : UKONIQ

    U.S.A
    FNCE 2024
    Not Confirmed
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    RLD : Yes

    TE Code :

    UMBRALISIB TOSYLATE

    TG Therapeutics

    Dosage Form : TABLET; ORAL

    Proprietary Name : UKONIQ

    Dosage Strength : EQ 200MG BASE

    Approval Date : 2021-02-05

    Application Number : 213176

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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