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    NDC 50090-5386-03 Nabumetone 750 mg/1 Details

    Nabumetone 750 mg/1

    Nabumetone is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is NABUMETONE.

    Product Information

    NDC 50090-5386
    Product ID 50090-5386_e12e92fc-1d46-43f0-85b4-1d2c99bea8c3
    Associated GPIs
    GCN Sequence Number 016575
    GCN Sequence Number Description nabumetone TABLET 750 MG ORAL
    HIC3 S2B
    HIC3 Description NSAIDS, CYCLOOXYGENASE INHIBITOR TYPE ANALGESICS
    GCN 32962
    HICL Sequence Number 006311
    HICL Sequence Number Description NABUMETONE
    Brand/Generic Generic
    Proprietary Name Nabumetone
    Proprietary Name Suffix n/a
    Non-Proprietary Name Nabumetone
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 750
    Active Ingredient Units mg/1
    Substance Name NABUMETONE
    Labeler Name A-S Medication Solutions
    Pharmaceutical Class Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078671
    Listing Certified Through 2024-12-31

    Package

    NDC 50090-5386-03 (50090538603)

    NDC Package Code 50090-5386-3
    Billing NDC 50090538603
    Package 60 TABLET, FILM COATED in 1 BOTTLE (50090-5386-3)
    Marketing Start Date 2020-11-20
    NDC Exclude Flag N
    Pricing Information N/A