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    NDC 69676-0063-05 Genexa Acetaminophen PM 500; 25 mg/1; mg/1 Details

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

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

    Product Information

    NDC 69676-0063
    Product ID 69676-0063_0c51f135-ce39-35e9-e063-6294a90acb8b
    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 Genexa Acetaminophen PM
    Proprietary Name Suffix Extra Strength
    Non-Proprietary Name Acetaminophen
    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 Genexa 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 69676-0063-05 (69676006305)

    NDC Package Code 69676-0063-5
    Billing NDC 69676006305
    Package 1 BOTTLE in 1 CARTON (69676-0063-5) / 50 TABLET, COATED in 1 BOTTLE
    Marketing Start Date 2022-02-17
    NDC Exclude Flag N
    Pricing Information N/A