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    NDC 63868-0210-20 Acetaminophen PM 500; 25 mg/1; mg/1 Details

    Acetaminophen PM 500; 25 mg/1; mg/1

    Acetaminophen PM is a ORAL TABLET, COATED in the HUMAN OTC DRUG category. It is labeled and distributed by CHAIN DRUG MARKETING ASSOCIATION INC. The primary component is ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE.

    Product Information

    NDC 63868-0210
    Product ID 63868-210_e1dcac61-3ba0-454c-8b2d-f2565a88eb70
    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 Acetaminophen PM
    Proprietary Name Suffix Extra Strength
    Non-Proprietary Name Acetaminophen, Diphenhydramine HCl
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 500; 25
    Active Ingredient Units mg/1; mg/1
    Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
    Labeler Name CHAIN DRUG MARKETING ASSOCIATION 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 63868-0210-20 (63868021020)

    NDC Package Code 63868-210-20
    Billing NDC 63868021020
    Package 1 BOTTLE, PLASTIC in 1 CARTON (63868-210-20) / 20 TABLET, COATED in 1 BOTTLE, PLASTIC
    Marketing Start Date 2007-12-17
    NDC Exclude Flag N
    Pricing Information N/A