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    NDC 42708-0045-21 PredniSONE 10 mg/1 Details

    PredniSONE 10 mg/1

    PredniSONE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by QPharma Inc. The primary component is PREDNISONE.

    Product Information

    NDC 42708-0045
    Product ID 42708-045_f28f7081-c253-4e6e-e053-2995a90a36bb
    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 PredniSONE
    Proprietary Name Suffix n/a
    Non-Proprietary Name PredniSONE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name PREDNISONE
    Labeler Name QPharma Inc
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA084122
    Listing Certified Through 2024-12-31

    Package

    NDC 42708-0045-21 (42708004521)

    NDC Package Code 42708-045-21
    Billing NDC 42708004521
    Package 21 TABLET in 1 BOTTLE, PLASTIC (42708-045-21)
    Marketing Start Date 2018-03-17
    NDC Exclude Flag N
    Pricing Information N/A