Search by Drug Name or NDC

    NDC 50580-0458-11 TYLENOL 325 mg/1 Details

    TYLENOL 325 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 50580-0458
    Product ID 50580-458_f780a8ee-c96d-03b3-e053-6394a90ae96e
    Associated GPIs 64200010000310
    GCN Sequence Number 004489
    GCN Sequence Number Description acetaminophen TABLET 325 MG ORAL
    HIC3 H3E
    HIC3 Description ANALGESIC/ANTIPYRETICS,NON-SALICYLATE
    GCN 16964
    HICL Sequence Number 001866
    HICL Sequence Number Description ACETAMINOPHEN
    Brand/Generic Brand
    Proprietary Name TYLENOL
    Proprietary Name Suffix Regular Strength
    Non-Proprietary Name acetaminophen
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 325
    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 50580-0458-11 (50580045811)

    NDC Package Code 50580-458-11
    Billing NDC 50580045811
    Package 10 BLISTER PACK in 1 CARTON (50580-458-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK
    Marketing Start Date 2020-07-17
    NDC Exclude Flag N
    Pricing Information N/A