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    NDC 11788-0004-10 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 AiPing Pharmaceutical, Inc.. The primary component is IBUPROFEN.

    Product Information

    NDC 11788-0004
    Product ID 11788-004_7c60fc45-3a27-9e52-e053-2a91aa0ab81e
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name IBUPROFEN
    Labeler Name AiPing Pharmaceutical, 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 ANDA206990
    Listing Certified Through 2023-12-31

    Package

    NDC 11788-0004-10 (11788000410)

    NDC Package Code 11788-004-10
    Billing NDC 11788000410
    Package 1000 TABLET, FILM COATED in 1 BOTTLE (11788-004-10)
    Marketing Start Date 2019-03-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 764ff65b-e6de-62e5-e053-2991aa0a94e5 Details

    Revised: 12/2018