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    NDC 60219-1707-03 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 Amneal Pharmaceuticals NY LLC. The primary component is PREDNISONE.

    Product Information

    NDC 60219-1707
    Product ID 60219-1707_5db920ec-a2c5-4564-b136-e8e210246c48
    Associated GPIs 22100045000320
    GCN Sequence Number 006749
    GCN Sequence Number Description prednisone TABLET 10 MG ORAL
    HIC3 P5A
    HIC3 Description GLUCOCORTICOIDS
    GCN 27172
    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 10
    Active Ingredient Units mg/1
    Substance Name PREDNISONE
    Labeler Name Amneal Pharmaceuticals NY LLC
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA213386
    Listing Certified Through 2024-12-31

    Package

    NDC 60219-1707-03 (60219170703)

    NDC Package Code 60219-1707-3
    Billing NDC 60219170703
    Package 10 BLISTER PACK in 1 CARTON (60219-1707-3) / 10 TABLET in 1 BLISTER PACK (60219-1707-2)
    Marketing Start Date 2020-06-24
    NDC Exclude Flag N
    Pricing Information N/A