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    NDC 11673-0050-58 up and up ibuprofen pm 38; 200 mg/1; mg/1 Details

    up and up ibuprofen pm 38; 200 mg/1; mg/1

    up and up ibuprofen pm is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Target Corporation. The primary component is DIPHENHYDRAMINE CITRATE; IBUPROFEN.

    Product Information

    NDC 11673-0050
    Product ID 11673-050_a7bb2e56-5bee-4872-8191-7821b0ac4859
    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 Generic
    Proprietary Name up and up ibuprofen pm
    Proprietary Name Suffix n/a
    Non-Proprietary Name diphenhydramine citrate and 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 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 ANDA079113
    Listing Certified Through 2024-12-31

    Package

    NDC 11673-0050-58 (11673005058)

    NDC Package Code 11673-050-58
    Billing NDC 11673005058
    Package 1 BOTTLE in 1 CARTON (11673-050-58) / 40 TABLET, FILM COATED in 1 BOTTLE
    Marketing Start Date 2009-07-24
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 0c764683-f3c9-4382-96be-d34b7a582aee Details

    Revised: 3/2022