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    NDC 61919-0326-30 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 Direct_Rx. The primary component is PREDNISONE.

    Product Information

    NDC 61919-0326
    Product ID 61919-326_f9b244f5-89d4-c2f0-e053-6294a90acd26
    Associated GPIs 22100045000325
    GCN Sequence Number 006751
    GCN Sequence Number Description prednisone TABLET 20 MG ORAL
    HIC3 P5A
    HIC3 Description GLUCOCORTICOIDS
    GCN 27174
    HICL Sequence Number 002879
    HICL Sequence Number Description PREDNISONE
    Brand/Generic Generic
    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 Direct_Rx
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA080356
    Listing Certified Through 2024-12-31

    Package

    NDC 61919-0326-30 (61919032630)

    NDC Package Code 61919-326-30
    Billing NDC 61919032630
    Package 30 TABLET in 1 BOTTLE (61919-326-30)
    Marketing Start Date 2022-09-19
    NDC Exclude Flag N
    Pricing Information N/A