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  5. NDC Package Code: 79481-0045-1 Pain Relief Extra Strength

NDC Package 79481-0045-1 Pain Relief Extra Strength

Acetaminophen Solution 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:
79481-0045-1
Package Description:
237 mL in 1 BOTTLE, PLASTIC
Product Code:
79481-0045
Proprietary Name:
Pain Relief Extra 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:
79481004501
NDC to RxNorm Crosswalk:
  • RxCUI: 307684 - acetaminophen 500 MG in 15 mL Oral Solution
  • RxCUI: 307684 - acetaminophen 33.3 MG/ML Oral Solution
  • RxCUI: 307684 - APAP 1000 MG per 30 ML Oral Solution
  • RxCUI: 307684 - APAP 167 MG per 5 ML Oral Solution
  • RxCUI: 307684 - APAP 33.3 MG/ML Oral Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Meijer Distribution, Inc.
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACETAMINOPHEN 1000 mg/30mL
    • Sample Package:
    No
    FDA Application Number:
    M013
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    04-14-2021
    Listing Expiration Date:
    12-31-2024
    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 79481-0045-1?

    The NDC Packaged Code 79481-0045-1 is assigned to a package of 237 ml in 1 bottle, plastic of Pain Relief Extra Strength, a human over the counter drug labeled by Meijer Distribution, Inc.. The product's dosage form is solution and is administered via oral form.

    Is NDC 79481-0045 included in the NDC Directory?

    Yes, Pain Relief Extra Strength with product code 79481-0045 is active and included in the NDC Directory. The product was first marketed by Meijer Distribution, Inc. on April 14, 2021 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 79481-0045-1?

    The 11-digit format is 79481004501. 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 5-4-1 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
    5-4-179481-0045-15-4-279481-0045-01