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    NDC 41250-0413-27 ibuprofen pm 38; 200 mg/1; mg/1 Details

    ibuprofen pm 38; 200 mg/1; mg/1

    ibuprofen pm is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Meijer Distribution Inc. The primary component is DIPHENHYDRAMINE CITRATE; IBUPROFEN.

    Product Information

    NDC 41250-0413
    Product ID 41250-413_35cf786a-8ee6-4bdf-8418-7c2d2f5c2f2d
    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 pm
    Proprietary Name Suffix n/a
    Non-Proprietary Name Diphenhydramine citrate, Ibuprofen
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 38; 200
    Active Ingredient Units mg/1; mg/1
    Substance Name DIPHENHYDRAMINE CITRATE; IBUPROFEN
    Labeler Name Meijer Distribution Inc
    Pharmaceutical Class Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA079113
    Listing Certified Through 2023-12-31

    Package

    NDC 41250-0413-27 (41250041327)

    NDC Package Code 41250-413-27
    Billing NDC 41250041327
    Package 1 BOTTLE in 1 CARTON (41250-413-27) / 80 TABLET, FILM COATED in 1 BOTTLE
    Marketing Start Date 2015-04-23
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 6ff80e79-afd2-4b05-a5ab-0794bcc5560f Details

    Revised: 12/2019