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  5. NDC Package Code: 50580-495-01 Tylenol Regular Strength

NDC Package 50580-495-01 Tylenol Regular Strength

Acetaminophen Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
50580-495-01
Package Description:
1 BOTTLE in 1 CARTON / 100 TABLET in 1 BOTTLE
Product Code:
50580-495
Proprietary Name:
Tylenol Regular Strength
Non-Proprietary Name:
Acetaminophen
Substance Name:
Acetaminophen
Usage Information:
This drug is used to treat mild to moderate pain (from headaches, menstrual periods, toothaches, backaches, osteoarthritis, or cold/flu aches and pains) and to reduce fever.
11-Digit NDC Billing Format:
50580049501
NDC to RxNorm Crosswalk:
  • RxCUI: 209387 - Tylenol Regular Strength 325 MG Oral Tablet
  • RxCUI: 209387 - acetaminophen 325 MG Oral Tablet [Tylenol]
  • RxCUI: 209387 - APAP 325 MG Oral Tablet [Tylenol]
  • RxCUI: 209387 - Tylenol 325 MG Oral Tablet
  • RxCUI: 313782 - acetaminophen 325 MG Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Johnson & Johnson Consumer Inc.
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACETAMINOPHEN 325 mg/1
    • Sample Package:
    No
    FDA Application Number:
    M013
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    12-01-2019
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50580-495-01?

    The NDC Packaged Code 50580-495-01 is assigned to a package of 1 bottle in 1 carton / 100 tablet in 1 bottle of Tylenol Regular Strength, a human over the counter drug labeled by Johnson & Johnson Consumer Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 50580-495 included in the NDC Directory?

    Yes, Tylenol Regular Strength with product code 50580-495 is active and included in the NDC Directory. The product was first marketed by Johnson & Johnson Consumer Inc. on December 01, 2019 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 50580-495-01?

    The 11-digit format is 50580049501. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-250580-495-015-4-250580-0495-01