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    NDC 00363-0756-40 Ibuprofen PM 25; 200 mg/1; mg/1 Details

    Ibuprofen PM 25; 200 mg/1; mg/1

    Ibuprofen PM is a ORAL CAPSULE, LIQUID FILLED in the HUMAN OTC DRUG category. It is labeled and distributed by Walgreens. The primary component is DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN.

    Product Information

    NDC 00363-0756
    Product ID 0363-0756_92c3c561-28da-4f48-846c-1e1bdf7a4b3f
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Ibuprofen PM
    Proprietary Name Suffix n/a
    Non-Proprietary Name IBUPROFEN, DIPHENHYDRAMINE HCL
    Product Type HUMAN OTC DRUG
    Dosage Form CAPSULE, LIQUID FILLED
    Route ORAL
    Active Ingredient Strength 25; 200
    Active Ingredient Units mg/1; mg/1
    Substance Name DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN
    Labeler Name Walgreens
    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 ANDA200888
    Listing Certified Through n/a

    Package

    NDC 00363-0756-40 (00363075640)

    NDC Package Code 0363-0756-40
    Billing NDC 00363075640
    Package 1 BOTTLE, PLASTIC in 1 BOX (0363-0756-40) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
    Marketing Start Date 2018-07-31
    NDC Exclude Flag N
    Pricing Information N/A