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    NDC 11673-0756-40 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 TARGET Corporation. The primary component is DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN.

    Product Information

    NDC 11673-0756
    Product ID 11673-756_895f988d-e624-440a-8863-9c4e060fa15b
    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 TARGET Corporation
    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 11673-0756-40 (11673075640)

    NDC Package Code 11673-756-40
    Billing NDC 11673075640
    Package 1 BOTTLE, PLASTIC in 1 BOX (11673-756-40) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
    Marketing Start Date 2018-03-31
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 5d2f2aad-af70-4ec3-89c9-4a11f8bcd115 Details

    Revised: 11/2022