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    Approved Drug Products containing 79174 listed in the FDA Orange Book. Original Data : FDA Website

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    Brand Name : IBUPROFEN

    India
    CPhI Worldwide, Milan
    Booth #22A34
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    Virtual BoothGranules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
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    RLD : No

    TE Code :

    IBUPROFEN

    Granules India Limited

    Dosage Form : TABLET; ORAL

    Proprietary Name : IBUPROFEN

    Dosage Strength : 200MG

    Approval Date : 2010-12-10

    Application Number : 79174

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

    Granules India

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