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    NDC 43063-0703-10 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 PD-Rx Pharmaceuticals, Inc.. The primary component is PREDNISONE.

    Product Information

    NDC 43063-0703
    Product ID 43063-703_05b87b34-516b-dfbb-e063-6394a90a0104
    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 PD-Rx Pharmaceuticals, Inc.
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA040362
    Listing Certified Through 2024-12-31

    Package

    NDC 43063-0703-10 (43063070310)

    NDC Package Code 43063-703-10
    Billing NDC 43063070310
    Package 10 TABLET in 1 BOTTLE, PLASTIC (43063-703-10)
    Marketing Start Date 2001-08-29
    NDC Exclude Flag N
    Pricing Information N/A