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    NDC 81522-0095-03 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 FSA STORE INC.. The primary component is ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE.

    Product Information

    NDC 81522-0095
    Product ID 81522-095_faca6208-9140-d434-e053-6394a90ad95a
    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 n/a
    Non-Proprietary Name Acetaminophen and Diphenhydramine Hydrochloride
    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 FSA STORE INC.
    Pharmaceutical Class Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through 2024-12-31

    Package

    NDC 81522-0095-03 (81522009503)

    NDC Package Code 81522-095-03
    Billing NDC 81522009503
    Package 1 BOTTLE, PLASTIC in 1 CARTON (81522-095-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
    Marketing Start Date 2023-05-02
    NDC Exclude Flag N
    Pricing Information N/A