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    NDC 68788-8184-03 prednisone 2.5 mg/1 Details

    prednisone 2.5 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 68788-8184
    Product ID 68788-8184_e3e5f077-a164-48f1-b95f-c6ab39585bcf
    Associated GPIs 22100045000310
    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 2.5
    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 ANDA209727
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-8184-03 (68788818403)

    NDC Package Code 68788-8184-3
    Billing NDC 68788818403
    Package 30 TABLET in 1 BOTTLE (68788-8184-3)
    Marketing Start Date 2022-05-06
    NDC Exclude Flag N
    Pricing Information N/A