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    NDC 68788-8116-01 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 Preferred Pharmaceuticals Inc.. The primary component is PREDNISONE.

    Product Information

    NDC 68788-8116
    Product ID 68788-8116_e23599f6-d9a4-459d-996d-4393e059ec4c
    Associated GPIs 22100045000320
    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 10
    Active Ingredient Units mg/1
    Substance Name PREDNISONE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA210525
    Listing Certified Through n/a

    Package

    NDC 68788-8116-01 (68788811601)

    NDC Package Code 68788-8116-1
    Billing NDC 68788811601
    Package 10 TABLET in 1 BOTTLE, PLASTIC (68788-8116-1)
    Marketing Start Date 2021-12-09
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 46aa0533-c1b4-4b2e-803b-a98eed07b8d9 Details

    Revised: 9/2022