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    NDC 71205-0357-06 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 Proficient Rx LP. The primary component is IBUPROFEN.

    Product Information

    NDC 71205-0357
    Product ID 71205-357_c18cb763-af0c-4cc2-b7df-520835c91884
    Associated GPIs 66100020000305
    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 Proficient Rx LP
    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 2024-12-31

    Package

    NDC 71205-0357-06 (71205035706)

    NDC Package Code 71205-357-06
    Billing NDC 71205035706
    Package 6 TABLET, FILM COATED in 1 BOTTLE (71205-357-06)
    Marketing Start Date 2019-11-12
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 798d33b0-5d7a-4445-8a51-2a3d336f744a Details

    Revised: 4/2022