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    NDC 55154-5382-00 Mycophenolate Mofetil 500 mg/1 Details

    Mycophenolate Mofetil 500 mg/1

    Mycophenolate Mofetil is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Cardinal Health 107, LLC. The primary component is MYCOPHENOLATE MOFETIL.

    Product Information

    NDC 55154-5382
    Product ID 55154-5382_700941b9-de3e-49c7-bca2-f85663cdf223
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Mycophenolate Mofetil
    Proprietary Name Suffix n/a
    Non-Proprietary Name mycophenolate mofetil
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name MYCOPHENOLATE MOFETIL
    Labeler Name Cardinal Health 107, LLC
    Pharmaceutical Class Antimetabolite Immunosuppressant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA065521
    Listing Certified Through n/a

    Package

    NDC 55154-5382-00 (55154538200)

    NDC Package Code 55154-5382-0
    Billing NDC 55154538200
    Package 10 BLISTER PACK in 1 BAG (55154-5382-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
    Marketing Start Date 2011-10-25
    NDC Exclude Flag N
    Pricing Information N/A