NDC Package 79903-005-12 All Day Pain Relief

Naproxen Sodium Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

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:
79903-005-12
Package Description:
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
All Day Pain Relief
Non-Proprietary Name:
Naproxen Sodium
Substance Name:
Naproxen Sodium
Usage Information:
Naproxen is used to relieve pain from various conditions. It also reduces pain, swelling, and joint stiffness caused by arthritis, bursitis, and gout attacks. This medication is known as a nonsteroidal anti-inflammatory drug (NSAID). It works by blocking your body's production of certain natural substances that cause inflammation. If you are treating a chronic condition such as arthritis, ask your doctor about non-drug treatments and/or using other medications to treat your pain. See also Warning section. Some brands of sustained-release naproxen take longer to be absorbed and are not recommended for pain that needs quick relief (such as during a gout attack). Ask your doctor or pharmacist if you have questions about your particular brand.
11-Digit NDC Billing Format:
79903000512
NDC to RxNorm Crosswalk:
  • RxCUI: 849574 - naproxen sodium 220 MG Oral Tablet
  • RxCUI: 849574 - naproxen sodium 220 MG (as naproxen 200 MG) Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Walmart Inc.
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA204872
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    10-22-2020
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    79903-005-101 BOTTLE, PLASTIC in 1 CARTON / 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    79903-005-25225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    79903-005-30300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    79903-005-751 BOTTLE, PLASTIC in 1 CARTON / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    79903-005-99100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 79903-005-12?

    The NDC Packaged Code 79903-005-12 is assigned to a package of 100 tablet, film coated in 1 bottle, plastic of All Day Pain Relief, a human over the counter drug labeled by Walmart Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 79903-005 included in the NDC Directory?

    Yes, All Day Pain Relief with product code 79903-005 is active and included in the NDC Directory. The product was first marketed by Walmart Inc. on October 22, 2020 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 79903-005-12?

    The 11-digit format is 79903000512. 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
    5-3-279903-005-125-4-279903-0005-12