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    NDC 68788-8166-02 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 Preferred Pharmaceuticals Inc.. The primary component is PREDNISONE.

    Product Information

    NDC 68788-8166
    Product ID 68788-8166_0e81640f-f171-44f3-bfbd-0f2c1d7c14df
    Associated GPIs 22100045000320
    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 Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA208412
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-8166-02 (68788816602)

    NDC Package Code 68788-8166-2
    Billing NDC 68788816602
    Package 21 TABLET in 1 BOTTLE (68788-8166-2)
    Marketing Start Date 2022-04-08
    NDC Exclude Flag N
    Pricing Information N/A