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    NDC 70934-0291-30 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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is PREDNISONE.

    Product Information

    NDC 70934-0291
    Product ID 70934-291_c8973905-80cb-2372-e053-2a95a90aea08
    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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA084122
    Listing Certified Through n/a

    Package

    NDC 70934-0291-30 (70934029130)

    NDC Package Code 70934-291-30
    Billing NDC 70934029130
    Package 30 TABLET in 1 BOTTLE, PLASTIC (70934-291-30)
    Marketing Start Date 2019-02-21
    NDC Exclude Flag N
    Pricing Information N/A