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    NDC 63323-0255-03 Methylprednisolone Sodium Succinate 40 mg/mL Details

    Methylprednisolone Sodium Succinate 40 mg/mL

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

    Product Information

    NDC 63323-0255
    Product ID 63323-255_dc369096-3042-4942-9aeb-bbdf98f35bb8
    Associated GPIs 22100030202105
    GCN Sequence Number 006732
    GCN Sequence Number Description methylprednisolone sod succ VIAL 40 MG INJECTION
    HIC3 P5A
    HIC3 Description GLUCOCORTICOIDS
    GCN 27032
    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 SODIUM SUCCINATE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
    Route INTRAMUSCULAR; INTRAVENOUS
    Active Ingredient Strength 40
    Active Ingredient Units mg/mL
    Substance Name METHYLPREDNISOLONE SODIUM SUCCINATE
    Labeler Name Fresenius Kabi USA, LLC
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA040583
    Listing Certified Through 2024-12-31

    Package

    NDC 63323-0255-03 (63323025503)

    NDC Package Code 63323-255-03
    Billing NDC 63323025503
    Package 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-255-03) / 1 mL in 1 VIAL, SINGLE-DOSE (63323-255-01)
    Marketing Start Date 2004-11-30
    NDC Exclude Flag N
    Pricing Information N/A