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    NDC 68071-1779-01 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 NuCare Pharmaceuticals,Inc.. The primary component is PREDNISONE.

    Product Information

    NDC 68071-1779
    Product ID 68071-1779_d59062ee-e444-022f-e053-2a95a90a7d20
    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 5
    Active Ingredient Units mg/1
    Substance Name PREDNISONE
    Labeler Name NuCare 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 68071-1779-01 (68071177901)

    NDC Package Code 68071-1779-1
    Billing NDC 68071177901
    Package 100 TABLET in 1 BOTTLE (68071-1779-1)
    Marketing Start Date 2018-10-26
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 7924d7e7-28bd-7e3b-e053-2a91aa0ae036 Details

    Revised: 1/2022