Search by Drug Name or NDC

    NDC 50580-0833-01 TYLENOL PM 1000; 50 mg/30mL; mg/30mL Details

    TYLENOL PM 1000; 50 mg/30mL; mg/30mL

    TYLENOL PM is a ORAL SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by Johnson & Johnson Consumer Inc.. The primary component is ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE.

    Product Information

    NDC 50580-0833
    Product ID 50580-833_f7b5e3b5-fc5a-e72f-e053-6294a90aa1e4
    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 TYLENOL PM
    Proprietary Name Suffix Extra Strength
    Non-Proprietary Name Acetaminophen and Diphenhydramine Hydrochloride
    Product Type HUMAN OTC DRUG
    Dosage Form SOLUTION
    Route ORAL
    Active Ingredient Strength 1000; 50
    Active Ingredient Units mg/30mL; mg/30mL
    Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
    Labeler Name Johnson & Johnson Consumer Inc.
    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 2024-12-31

    Package

    NDC 50580-0833-01 (50580083301)

    NDC Package Code 50580-833-01
    Billing NDC 50580083301
    Package 240 mL in 1 BOTTLE (50580-833-01)
    Marketing Start Date 2018-06-25
    NDC Exclude Flag N
    Pricing Information N/A