Search by Drug Name or NDC

    NDC 68788-7080-05 Ibuprofen 800 mg/1 Details

    Ibuprofen 800 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 68788-7080
    Product ID 68788-7080_60282a42-bd45-4577-83a4-1d5e5250adff
    Associated GPIs 66100020000340
    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 800
    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 68788-7080-05 (68788708005)

    NDC Package Code 68788-7080-5
    Billing NDC 68788708005
    Package 50 TABLET, FILM COATED in 1 BOTTLE (68788-7080-5)
    Marketing Start Date 2018-01-11
    NDC Exclude Flag N
    Pricing Information N/A