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    NDC 41250-0285-22 Ibuprofen PM 25; 200 mg/1; mg/1 Details

    Ibuprofen PM 25; 200 mg/1; mg/1

    Ibuprofen PM is a ORAL CAPSULE, LIQUID FILLED in the HUMAN OTC DRUG category. It is labeled and distributed by MEIJER DISTRIBUTION INC.. The primary component is DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN.

    Product Information

    NDC 41250-0285
    Product ID 41250-285_eb64f59f-eef1-8517-e053-2a95a90a3948
    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 IBUPROFEN, DIPHENHYDRAMINE HCL
    Product Type HUMAN OTC DRUG
    Dosage Form CAPSULE, LIQUID FILLED
    Route ORAL
    Active Ingredient Strength 25; 200
    Active Ingredient Units mg/1; mg/1
    Substance Name DIPHENHYDRAMINE HYDROCHLORIDE; 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 ANDA090397
    Listing Certified Through 2024-12-31

    Package

    NDC 41250-0285-22 (41250028522)

    NDC Package Code 41250-285-22
    Billing NDC 41250028522
    Package 120 CAPSULE, LIQUID FILLED in 1 BOTTLE (41250-285-22)
    Marketing Start Date 2021-02-24
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL bb7701aa-f482-69e7-e053-2995a90a71b8 Details

    Revised: 10/2022