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    NDC 72789-0229-01 Hydrocortisone 20 mg/1 Details

    Hydrocortisone 20 mg/1

    Hydrocortisone is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is HYDROCORTISONE.

    Product Information

    NDC 72789-0229
    Product ID 72789-229_f889231a-b25f-2ec4-e053-6294a90a6018
    Associated GPIs 22100025000310
    GCN Sequence Number 006704
    GCN Sequence Number Description hydrocortisone TABLET 20 MG ORAL
    HIC3 P5A
    HIC3 Description GLUCOCORTICOIDS
    GCN 26782
    HICL Sequence Number 002867
    HICL Sequence Number Description HYDROCORTISONE
    Brand/Generic Generic
    Proprietary Name Hydrocortisone
    Proprietary Name Suffix n/a
    Non-Proprietary Name Hydrocortisone
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name HYDROCORTISONE
    Labeler Name PD-Rx Pharmaceuticals, Inc.
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207029
    Listing Certified Through 2024-12-31

    Package

    NDC 72789-0229-01 (72789022901)

    NDC Package Code 72789-229-01
    Billing NDC 72789022901
    Package 100 TABLET in 1 BOTTLE, PLASTIC (72789-229-01)
    Marketing Start Date 2022-12-22
    NDC Exclude Flag N
    Pricing Information N/A