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    NDC 72927-0805-01 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 Strides Consumer LLC. The primary component is IBUPROFEN.

    Product Information

    NDC 72927-0805
    Product ID 72927-805_81537956-fe44-4175-bbcf-eb0aa383dc86
    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, COATED
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name IBUPROFEN
    Labeler Name Strides Consumer 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 ANDA207052
    Listing Certified Through 2024-12-31

    Package

    NDC 72927-0805-01 (72927080501)

    NDC Package Code 72927-805-01
    Billing NDC 72927080501
    Package 1 BOTTLE in 1 CARTON (72927-805-01) / 120 TABLET, COATED in 1 BOTTLE
    Marketing Start Date 2019-09-10
    NDC Exclude Flag N
    Pricing Information N/A
    << 72924-0001-01 72927-0805-02 >>

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