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    NDC 50844-0235-15 Pain Reliever PM 500; 25 mg/1; mg/1 Details

    Pain Reliever PM 500; 25 mg/1; mg/1

    Pain Reliever PM is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by L.N.K. International, Inc.. The primary component is ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE.

    Product Information

    NDC 50844-0235
    Product ID 50844-235_9f771d40-365d-4b1a-9dcb-f167ffd036ee
    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 Pain Reliever PM
    Proprietary Name Suffix Extra Strength
    Non-Proprietary Name Acetaminophen, Diphenhydramine HCl
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 500; 25
    Active Ingredient Units mg/1; mg/1
    Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
    Labeler Name L.N.K. International, Inc.
    Pharmaceutical Class Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH DRUG
    Application Number M013
    Listing Certified Through 2024-12-31

    Package

    NDC 50844-0235-15 (50844023515)

    NDC Package Code 50844-235-15
    Billing NDC 50844023515
    Package 1 BOTTLE, PLASTIC in 1 CARTON (50844-235-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    Marketing Start Date 1994-05-15
    NDC Exclude Flag N
    Pricing Information N/A