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    NDC 41250-0074-78 ibuprofen 200 mg/1 Details

    ibuprofen 200 mg/1

    ibuprofen is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Meijer Distribution Inc. The primary component is IBUPROFEN.

    Product Information

    NDC 41250-0074
    Product ID 41250-074_06e2a025-460a-48c2-8e87-1de554609552
    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
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ibuprofen
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name IBUPROFEN
    Labeler Name Meijer Distribution Inc
    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 ANDA077349
    Listing Certified Through 2024-12-31

    Package

    NDC 41250-0074-78 (41250007478)

    NDC Package Code 41250-074-78
    Billing NDC 41250007478
    Package 1 BOTTLE in 1 CARTON (41250-074-78) / 100 TABLET, FILM COATED in 1 BOTTLE
    Marketing Start Date 2006-06-21
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 8d4cb97a-3b36-423e-85f2-75d23a675601 Details

    Revised: 2/2019