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    NDC 51655-0701-18 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 Northwind Pharmaceuticals, LLC. The primary component is PREDNISONE.

    Product Information

    NDC 51655-0701
    Product ID 51655-701_f7e47fd0-041e-82e0-e053-6394a90a8806
    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 20
    Active Ingredient Units mg/1
    Substance Name PREDNISONE
    Labeler Name Northwind Pharmaceuticals, LLC
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA087342
    Listing Certified Through 2024-12-31

    Package

    NDC 51655-0701-18 (51655070118)

    NDC Package Code 51655-701-18
    Billing NDC 51655070118
    Package 18 TABLET in 1 BOTTLE, PLASTIC (51655-701-18)
    Marketing Start Date 2021-06-10
    NDC Exclude Flag N
    Pricing Information N/A