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    NDC 41163-0050-27 equaline ibuprofen pm 38; 200 mg/1; mg/1 Details

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

    equaline ibuprofen pm is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by United Natural Foods, Inc. dba UNFI. The primary component is DIPHENHYDRAMINE CITRATE; IBUPROFEN.

    Product Information

    NDC 41163-0050
    Product ID 41163-050_240bca28-8f82-4586-9917-eac30577cd29
    Associated GPIs 92200040002015
    GCN Sequence Number 062493
    GCN Sequence Number Description ibuprofen/diphenhydramine cit TABLET 200MG-38MG ORAL
    HIC3 S2S
    HIC3 Description ANALGESIC,NSAID-1ST GEN.ANTIHISTAMINE,SEDATIVE CMB
    GCN 98268
    HICL Sequence Number 034634
    HICL Sequence Number Description IBUPROFEN/DIPHENHYDRAMINE CITRATE
    Brand/Generic Generic
    Proprietary Name equaline 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 United Natural Foods, Inc. dba UNFI
    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 2024-12-31

    Package

    NDC 41163-0050-27 (41163005027)

    NDC Package Code 41163-050-27
    Billing NDC 41163005027
    Package 1 BOTTLE in 1 CARTON (41163-050-27) / 80 TABLET, FILM COATED in 1 BOTTLE
    Marketing Start Date 2009-03-02
    NDC Exclude Flag N
    Pricing Information N/A