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    Approved Drug Products containing 22311 listed in the FDA Orange Book. Original Data : FDA Website

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    Brand Name : MOZOBIL

    France
    AAPS 2024
    Not Confirmed
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    Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
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    RLD : Yes

    TE Code : AP

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    Dosage Form : SOLUTION; SUBCUTANEOUS

    Proprietary Name : MOZOBIL

    Dosage Strength : 24MG/1.2ML (20MG/ML)

    Approval Date : 2008-12-15

    Application Number : 22311

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

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