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    NDC 68788-7752-00 PREDNISONE 20 mg/1 Details

    PREDNISONE 20 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 68788-7752
    Product ID 68788-7752_1c897a3c-b971-4d04-bf9b-1a7c77c497e0
    Associated GPIs 22100045000325
    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 20
    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 ANDA210525
    Listing Certified Through 2022-12-31

    Package

    NDC 68788-7752-00 (68788775200)

    NDC Package Code 68788-7752-0
    Billing NDC 68788775200
    Package 18 TABLET in 1 BOTTLE, PLASTIC (68788-7752-0)
    Marketing Start Date 2020-07-01
    NDC Exclude Flag N
    Pricing Information N/A