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    NDC 51672-2138-08 Ibuprofen 100 mg/5mL Details

    Ibuprofen 100 mg/5mL

    Ibuprofen is a ORAL SUSPENSION in the HUMAN OTC DRUG category. It is labeled and distributed by Taro Pharmaceuticals U.S.A., Inc.. The primary component is IBUPROFEN.

    Product Information

    NDC 51672-2138
    Product ID 51672-2138_82e13eb7-a786-4727-9f5d-956095aabad6
    Associated GPIs 66100020001820
    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 SUSPENSION
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/5mL
    Substance Name IBUPROFEN
    Labeler Name Taro Pharmaceuticals U.S.A., Inc.
    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 ANDA209207
    Listing Certified Through 2023-12-31

    Package

    NDC 51672-2138-08 (51672213808)

    NDC Package Code 51672-2138-8
    Billing NDC 51672213808
    Package 1 BOTTLE in 1 CARTON (51672-2138-8) / 120 mL in 1 BOTTLE
    Marketing Start Date 2018-09-12
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 80a70da7-371b-4ad6-b480-dc165704dd25 Details

    Revised: 9/2018