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    NDC 63868-0268-25 Ibuprofen 200 mg/1 Details

    Ibuprofen 200 mg/1

    Ibuprofen is a ORAL TABLET, COATED in the HUMAN OTC DRUG category. It is labeled and distributed by CHAIN DRUG MARKETING ASSOCIATION INC. The primary component is IBUPROFEN.

    Product Information

    NDC 63868-0268
    Product ID 63868-268_d07197cb-9b39-82f5-e053-2995a90a1e3b
    Associated GPIs
    GCN Sequence Number 008346
    GCN Sequence Number Description ibuprofen TABLET 200 MG ORAL
    HIC3 S2B
    HIC3 Description NSAIDS, CYCLOOXYGENASE INHIBITOR TYPE ANALGESICS
    GCN 35743
    HICL Sequence Number 003723
    HICL Sequence Number Description IBUPROFEN
    Brand/Generic Generic
    Proprietary Name Ibuprofen
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ibuprofen
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name IBUPROFEN
    Labeler Name CHAIN DRUG MARKETING ASSOCIATION 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 ANDA079174
    Listing Certified Through 2024-12-31

    Package

    NDC 63868-0268-25 (63868026825)

    NDC Package Code 63868-268-25
    Billing NDC 63868026825
    Package 250 TABLET, COATED in 1 BOTTLE, PLASTIC (63868-268-25)
    Marketing Start Date 2021-05-31
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL c13455a3-307a-4fe1-e053-2a95a90adf8e Details

    Revised: 11/2021