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    NDC 70121-1001-05 Methylprednisolone Sodium Succinate 125 mg/2mL Details

    Methylprednisolone Sodium Succinate 125 mg/2mL

    Methylprednisolone Sodium Succinate is a INTRAMUSCULAR; INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals LLC. The primary component is METHYLPREDNISOLONE SODIUM SUCCINATE.

    Product Information

    NDC 70121-1001
    Product ID 70121-1001_2aa217c3-8a65-429b-9ec4-922151926fe9
    Associated GPIs 22100030202110
    GCN Sequence Number 006730
    GCN Sequence Number Description methylprednisolone sod succ VIAL 125 MG INJECTION
    HIC3 P5A
    HIC3 Description GLUCOCORTICOIDS
    GCN 27031
    HICL Sequence Number 002876
    HICL Sequence Number Description METHYLPREDNISOLONE SODIUM SUCCINATE
    Brand/Generic Generic
    Proprietary Name Methylprednisolone Sodium Succinate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Methylprednisolone
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
    Route INTRAMUSCULAR; INTRAVENOUS
    Active Ingredient Strength 125
    Active Ingredient Units mg/2mL
    Substance Name METHYLPREDNISOLONE SODIUM SUCCINATE
    Labeler Name Amneal Pharmaceuticals LLC
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207549
    Listing Certified Through 2024-12-31

    Package

    NDC 70121-1001-05 (70121100105)

    NDC Package Code 70121-1001-5
    Billing NDC 70121100105
    Package 25 VIAL in 1 CARTON (70121-1001-5) / 2 mL in 1 VIAL (70121-1001-1)
    Marketing Start Date 2016-11-11
    NDC Exclude Flag N
    Pricing Information N/A