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    NDC 50580-0590-06 TYLENOL 500 mg/1 Details

    TYLENOL 500 mg/1

    TYLENOL is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Johnson & Johnson Consumer Inc.. The primary component is ACETAMINOPHEN.

    Product Information

    NDC 50580-0590
    Product ID 50580-590_ff16d4d6-393d-b55b-e053-6394a90afdea
    Associated GPIs
    GCN Sequence Number 004490
    GCN Sequence Number Description acetaminophen TABLET 500 MG ORAL
    HIC3 H3E
    HIC3 Description ANALGESIC/ANTIPYRETICS,NON-SALICYLATE
    GCN 16965
    HICL Sequence Number 001866
    HICL Sequence Number Description ACETAMINOPHEN
    Brand/Generic Brand
    Proprietary Name TYLENOL
    Proprietary Name Suffix Extra Strength
    Non-Proprietary Name acetaminophen
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name ACETAMINOPHEN
    Labeler Name Johnson & Johnson Consumer Inc.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH NOT FINAL
    Application Number part343
    Listing Certified Through 2024-12-31

    Package

    NDC 50580-0590-06 (50580059006)

    NDC Package Code 50580-590-06
    Billing NDC 50580059006
    Package 1 BOTTLE in 1 CARTON (50580-590-06) / 225 TABLET, FILM COATED in 1 BOTTLE
    Marketing Start Date 2020-07-31
    NDC Exclude Flag N
    Pricing Information N/A