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    NDC 58602-0708-01 Ibuprofen 200 mg/1 Details

    Ibuprofen 200 mg/1

    Ibuprofen is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Aurohealth LLC. The primary component is IBUPROFEN.

    Product Information

    NDC 58602-0708
    Product ID 58602-708_09bd3935-526d-4ad1-898a-4f0d9499ebb9
    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
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name IBUPROFEN
    Labeler Name Aurohealth LLC
    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 ANDA208865
    Listing Certified Through 2024-12-31

    Package

    NDC 58602-0708-01 (58602070801)

    NDC Package Code 58602-708-01
    Billing NDC 58602070801
    Package 1 BOTTLE, PLASTIC in 1 CARTON (58602-708-01) / 24 TABLET in 1 BOTTLE, PLASTIC
    Marketing Start Date 2022-03-22
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 09bd3935-526d-4ad1-898a-4f0d9499ebb9 Details

    Revised: 3/2022