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    NDC 30142-0495-82 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 Kroger Company. The primary component is IBUPROFEN.

    Product Information

    NDC 30142-0495
    Product ID 30142-495_be5bc6fe-e14d-438f-bab4-0e0a8d1728cd
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name IBUPROFEN
    Labeler Name Kroger Company
    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 ANDA072096
    Listing Certified Through n/a

    Package

    NDC 30142-0495-82 (30142049582)

    NDC Package Code 30142-495-82
    Billing NDC 30142049582
    Package 200 TABLET, FILM COATED in 1 BOTTLE (30142-495-82)
    Marketing Start Date 2019-11-14
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL a1a23c80-d6af-4e8e-a4a0-8366261bc92b Details

    Revised: 11/2022