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    NDC 41250-0801-82 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 Meijer, Inc.. The primary component is IBUPROFEN.

    Product Information

    NDC 41250-0801
    Product ID 41250-801_ae419268-b2f9-4693-8b1d-f43201a00df4
    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 Meijer, 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 ANDA072096
    Listing Certified Through 2023-12-31

    Package

    NDC 41250-0801-82 (41250080182)

    NDC Package Code 41250-801-82
    Billing NDC 41250080182
    Package 2 BOTTLE in 1 CARTON (41250-801-82) / 100 TABLET, FILM COATED in 1 BOTTLE
    Marketing Start Date 2017-07-12
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 188f8ca6-c9c2-417f-a461-fa0eabf3b11c Details

    Revised: 12/2019