NDC Package 29485-1013-2 Aleve

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

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

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:
29485-1013-2
Package Description:
2 POUCH in 1 BLISTER PACK / 1 TABLET in 1 POUCH
Product Code:
Proprietary Name:
Aleve
Non-Proprietary Name:
Naproxen Sodium Tablet
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:
29485101302
Product Type:
Human Otc Drug
Labeler Name:
Lil' Drug Store Products, 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):
Sample Package:
No
FDA Application Number:
NDA020204
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
04-30-2002
End Marketing Date:
09-30-2025
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.

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Frequently Asked Questions

What is NDC 29485-1013-2?

The NDC Packaged Code 29485-1013-2 is assigned to a package of 2 pouch in 1 blister pack / 1 tablet in 1 pouch of Aleve, a human over the counter drug labeled by Lil' Drug Store Products, Inc.. The product's dosage form is tablet and is administered via oral form.

Is NDC 29485-1013 included in the NDC Directory?

Yes, Aleve with product code 29485-1013 is active and included in the NDC Directory. The product was first marketed by Lil' Drug Store Products, Inc. on April 30, 2002.

What is the 11-digit format for NDC 29485-1013-2?

The 11-digit format is 29485101302. 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
5-4-129485-1013-25-4-229485-1013-02