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    NDC 59726-0046-30 Ibuprofen 200 mg/1 Details

    Ibuprofen 200 mg/1

    Ibuprofen is a ORAL CAPSULE, LIQUID FILLED in the HUMAN OTC DRUG category. It is labeled and distributed by P & L Development, LLC. The primary component is IBUPROFEN.

    Product Information

    NDC 59726-0046
    Product ID 59726-046_c6feb159-979a-479e-ae12-3b80c7e2135d
    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 CAPSULE, LIQUID FILLED
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name IBUPROFEN
    Labeler Name P & L Development, 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 ANDA207753
    Listing Certified Through 2024-12-31

    Package

    NDC 59726-0046-30 (59726004630)

    NDC Package Code 59726-046-30
    Billing NDC 59726004630
    Package 1 BOTTLE, PLASTIC in 1 BOX (59726-046-30) / 30 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
    Marketing Start Date 2020-12-04
    NDC Exclude Flag N
    Pricing Information N/A