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    NDC 68382-0919-77 methylprednisolone 32 mg/1 Details

    methylprednisolone 32 mg/1

    methylprednisolone is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is METHYLPREDNISOLONE.

    Product Information

    NDC 68382-0919
    Product ID 68382-919_67799c09-3d66-47e4-99f4-7dca4fc3344c
    Associated GPIs 22100030000330
    GCN Sequence Number 006740
    GCN Sequence Number Description methylprednisolone TABLET 32 MG ORAL
    HIC3 P5A
    HIC3 Description GLUCOCORTICOIDS
    GCN 27055
    HICL Sequence Number 002877
    HICL Sequence Number Description METHYLPREDNISOLONE
    Brand/Generic Generic
    Proprietary Name methylprednisolone
    Proprietary Name Suffix n/a
    Non-Proprietary Name methylprednisolone
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 32
    Active Ingredient Units mg/1
    Substance Name METHYLPREDNISOLONE
    Labeler Name Zydus Pharmaceuticals USA Inc.
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA206751
    Listing Certified Through 2024-12-31

    Package

    NDC 68382-0919-77 (68382091977)

    NDC Package Code 68382-919-77
    Billing NDC 68382091977
    Package 10 BLISTER PACK in 1 CARTON (68382-919-77) / 10 TABLET in 1 BLISTER PACK (68382-919-30)
    Marketing Start Date 2018-05-01
    NDC Exclude Flag N
    Pricing Information N/A