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    NDC 00573-0164-55 ADVIL PM 38; 200 mg/1; mg/1 Details

    ADVIL PM 38; 200 mg/1; mg/1

    ADVIL PM is a ORAL TABLET, COATED in the HUMAN OTC DRUG category. It is labeled and distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. The primary component is DIPHENHYDRAMINE CITRATE; IBUPROFEN.

    Product Information

    NDC 00573-0164
    Product ID 0573-0164_84782dbd-48de-47fc-96c0-bb9834d8c966
    Associated GPIs 60309902400320
    GCN Sequence Number 062493
    GCN Sequence Number Description ibuprofen/diphenhydramine cit TABLET 200MG-38MG ORAL
    HIC3 S2S
    HIC3 Description ANALGESIC,NSAID-1ST GEN.ANTIHISTAMINE,SEDATIVE CMB
    GCN 98268
    HICL Sequence Number 034634
    HICL Sequence Number Description IBUPROFEN/DIPHENHYDRAMINE CITRATE
    Brand/Generic Brand
    Proprietary Name ADVIL PM
    Proprietary Name Suffix n/a
    Non-Proprietary Name diphenhydramine citrate and ibuprofen
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 38; 200
    Active Ingredient Units mg/1; mg/1
    Substance Name DIPHENHYDRAMINE CITRATE; IBUPROFEN
    Labeler Name GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
    Pharmaceutical Class Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA021394
    Listing Certified Through 2024-12-31

    Package

    NDC 00573-0164-55 (00573016455)

    NDC Package Code 0573-0164-55
    Billing NDC 00573016455
    Package 50 POUCH in 1 TRAY (0573-0164-55) / 2 TABLET, COATED in 1 POUCH
    Marketing Start Date 2005-12-21
    NDC Exclude Flag N
    Pricing Information N/A