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    NDC 00363-0050-82 Ibuprofen PM 38; 200 mg/1; mg/1 Details

    Ibuprofen PM 38; 200 mg/1; mg/1

    Ibuprofen PM is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Walgreen Company. The primary component is DIPHENHYDRAMINE CITRATE; IBUPROFEN.

    Product Information

    NDC 00363-0050
    Product ID 0363-0050_0f668c99-f879-470b-8c3e-3fe1fef10837
    Associated GPIs 48991003101835
    GCN Sequence Number 002706
    GCN Sequence Number Description mag hydrox/aluminum hyd/simeth ORAL SUSP 400-400-40 ORAL
    HIC3 D4B
    HIC3 Description ANTACIDS
    GCN 63915
    HICL Sequence Number 001168
    HICL Sequence Number Description MAGNESIUM HYDROXIDE/ALUMINUM HYDROXIDE/SIMETHICONE
    Brand/Generic Generic
    Proprietary Name Ibuprofen PM
    Proprietary Name Suffix n/a
    Non-Proprietary Name diphenhydramine citrate, ibuprofen
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 38; 200
    Active Ingredient Units mg/1; mg/1
    Substance Name DIPHENHYDRAMINE CITRATE; IBUPROFEN
    Labeler Name Walgreen Company
    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 ANDA
    Application Number ANDA079113
    Listing Certified Through 2024-12-31

    Package

    NDC 00363-0050-82 (00363005082)

    NDC Package Code 0363-0050-82
    Billing NDC 00363005082
    Package 200 TABLET, FILM COATED in 1 BOTTLE (0363-0050-82)
    Marketing Start Date 2017-09-21
    NDC Exclude Flag N
    Pricing Information N/A