Search by Drug Name or NDC

    NDC 11673-0685-34 up and up ibuprofen 100 mg/5mL Details

    up and up ibuprofen 100 mg/5mL

    up and up ibuprofen is a ORAL SUSPENSION in the HUMAN OTC DRUG category. It is labeled and distributed by Target Corporation. The primary component is IBUPROFEN.

    Product Information

    NDC 11673-0685
    Product ID 11673-685_b99f3447-0a91-4118-92f1-e6fd3f0c9a27
    Associated GPIs 66100020001820
    GCN Sequence Number 012080
    GCN Sequence Number Description ibuprofen ORAL SUSP 100 MG/5ML ORAL
    HIC3 S2B
    HIC3 Description NSAIDS, CYCLOOXYGENASE INHIBITOR TYPE ANALGESICS
    GCN 35930
    HICL Sequence Number 003723
    HICL Sequence Number Description IBUPROFEN
    Brand/Generic Generic
    Proprietary Name up and up ibuprofen
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ibuprofen
    Product Type HUMAN OTC DRUG
    Dosage Form SUSPENSION
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/5mL
    Substance Name IBUPROFEN
    Labeler Name Target Corporation
    Pharmaceutical Class Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA074937
    Listing Certified Through 2024-12-31

    Package

    NDC 11673-0685-34 (11673068534)

    NDC Package Code 11673-685-34
    Billing NDC 11673068534
    Package 1 BOTTLE in 1 CARTON (11673-685-34) / 237 mL in 1 BOTTLE
    Marketing Start Date 2011-03-12
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 6e0330ac-a111-4574-9197-d7aab33b8608 Details

    Revised: 10/2017