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    NDC 72789-0040-30 Nabumetone 750 mg/1 Details

    Nabumetone 750 mg/1

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

    Product Information

    NDC 72789-0040
    Product ID 72789-040_fe4577fa-39e3-ccad-e053-6294a90a9ee4
    Associated GPIs 66100055000330
    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
    Route ORAL
    Active Ingredient Strength 750
    Active Ingredient Units mg/1
    Substance Name NABUMETONE
    Labeler Name PD-Rx Pharmaceuticals, Inc.
    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 ANDA078420
    Listing Certified Through 2024-12-31

    Package

    NDC 72789-0040-30 (72789004030)

    NDC Package Code 72789-040-30
    Billing NDC 72789004030
    Package 30 TABLET in 1 BOTTLE, PLASTIC (72789-040-30)
    Marketing Start Date 2019-12-17
    NDC Exclude Flag N
    Pricing Information N/A