Search by Drug Name or NDC

    NDC 68788-7114-09 Ibuprofen 400 mg/1 Details

    Ibuprofen 400 mg/1

    Ibuprofen is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is IBUPROFEN.

    Product Information

    NDC 68788-7114
    Product ID 68788-7114_c3fa33e1-bf30-4701-ac67-f6f201646e5f
    Associated GPIs 66100020000320
    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 PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 400
    Active Ingredient Units mg/1
    Substance Name IBUPROFEN
    Labeler Name Preferred Pharmaceuticals 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 ANDA091625
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7114-09 (68788711409)

    NDC Package Code 68788-7114-9
    Billing NDC 68788711409
    Package 90 TABLET, FILM COATED in 1 BOTTLE (68788-7114-9)
    Marketing Start Date 2018-03-12
    NDC Exclude Flag N
    Pricing Information N/A