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    NDC 58602-0743-29 Aurophen PM Extra Strength 500; 25 mg/1; mg/1 Details

    Aurophen PM Extra Strength 500; 25 mg/1; mg/1

    Aurophen PM Extra Strength is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Aurohealth LLC. The primary component is ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE.

    Product Information

    NDC 58602-0743
    Product ID 58602-743_b9e2bb05-d7c7-46fc-abd4-35b542239c91
    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 Aurophen PM Extra Strength
    Proprietary Name Suffix n/a
    Non-Proprietary Name Acetaminophen and Diphenhydramine HCl
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 500; 25
    Active Ingredient Units mg/1; mg/1
    Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
    Labeler Name Aurohealth LLC
    Pharmaceutical Class Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH NOT FINAL
    Application Number part343
    Listing Certified Through 2023-12-31

    Package

    NDC 58602-0743-29 (58602074329)

    NDC Package Code 58602-743-29
    Billing NDC 58602074329
    Package 150 TABLET in 1 BOTTLE (58602-743-29)
    Marketing Start Date 2016-02-24
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 994351af-0c08-436f-a623-149ff7c7c463 Details

    Revised: 12/2020