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    NDC 70518-2115-02 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 REMEDYREPACK INC.. The primary component is PREDNISONE.

    Product Information

    NDC 70518-2115
    Product ID 70518-2115_f654bb0d-4873-1b21-e053-2a95a90a2369
    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 10
    Active Ingredient Units mg/1
    Substance Name PREDNISONE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA088832
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2115-02 (70518211502)

    NDC Package Code 70518-2115-2
    Billing NDC 70518211502
    Package 30 TABLET in 1 BOTTLE, PLASTIC (70518-2115-2)
    Marketing Start Date 2020-08-21
    NDC Exclude Flag N
    Pricing Information N/A