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  5. NDC Package Code: 67751-167-04 Tylenol Extra Strength

NDC Package 67751-167-04 Tylenol Extra Strength

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
67751-167-04
Package Description:
12 POUCH in 1 TRAY / 1 TABLET, FILM COATED in 1 POUCH
Product Code:
67751-167
Proprietary Name:
Tylenol Extra Strength
Usage Information:
Do not take more than directed (see overdose warning) adults and children 12 years and over• take 2 caplets every 6 hours while symptoms last• do not take more than 6 caplets in 24 hours, unless directed by a doctor• do not use for more than 10 days unless directed by a doctor children under 12 years ask a doctor
11-Digit NDC Billing Format:
67751016704
NDC to RxNorm Crosswalk:
  • RxCUI: 198440 - acetaminophen 500 MG Oral Tablet
  • RxCUI: 198440 - APAP 500 MG Oral Tablet
  • RxCUI: 209459 - Tylenol Extra Strength 500 MG Oral Tablet
  • RxCUI: 209459 - acetaminophen 500 MG Oral Tablet [Tylenol]
  • RxCUI: 209459 - APAP 500 MG Oral Tablet [Tylenol]
    • Labeler Name:
    Navajo Manufacturing Company Inc.
    Sample Package:
    No
    Start Marketing Date:
    12-04-2017
    Listing Expiration Date:
    12-31-2019
    Exclude Flag:
    I
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    67751-167-011 POUCH in 1 CARTON / 2 TABLET, FILM COATED in 1 POUCH
    67751-167-021 POUCH in 1 CARTON / 4 TABLET, FILM COATED in 1 POUCH
    67751-167-032 TRAY in 1 POUCH / 12 TABLET in 1 TRAY

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 67751-167-04?

    The NDC Packaged Code 67751-167-04 is assigned to a package of 12 pouch in 1 tray / 1 tablet, film coated in 1 pouch of Tylenol Extra Strength, labeled by Navajo Manufacturing Company Inc.. The product's dosage form is and is administered via form.

    Is NDC 67751-167 included in the NDC Directory?

    No, Tylenol Extra Strength with product code 67751-167 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Navajo Manufacturing Company Inc. on December 04, 2017 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 67751-167-04?

    The 11-digit format is 67751016704. 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
    5-3-267751-167-045-4-267751-0167-04