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    NDC 68788-7372-08 Prednisone 5 mg/1 Details

    Prednisone 5 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 68788-7372
    Product ID 68788-7372_cff38d44-141c-4d60-98ba-3ebae35cc93b
    Associated GPIs 22100045000315
    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 5
    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 ANDA040362
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7372-08 (68788737208)

    NDC Package Code 68788-7372-8
    Billing NDC 68788737208
    Package 21 TABLET in 1 BOTTLE (68788-7372-8)
    Marketing Start Date 2017-02-21
    NDC Exclude Flag N
    Pricing Information N/A