Advil
NDC Package 52904-786-50

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

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

Advil is a medication used as Pain reliever/Fever reducer. Marketed by Wyeth Pharmaceuticals Company, this product is identified by NDC 52904-786 and is authorized under FDA application NDA018989.

Identification & Billing

NDC Package Code
52904-786-50
Package Description
50 POUCH in 1 CASE / 2 TABLET, COATED in 1 POUCH
Product Code
52904-786
11-Digit Billing Format
52904078650
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Advil
Dosage Form
-
Usage Information
This product is used as Pain reliever/Fever reducer. Temporarily relieves minor aches and pains due to:headachetoothachebackachemenstrual crampsthe common coldmuscular achesminor pain of arthritistemporarily reduces fever

Regulatory & Marketing

Labeler Name
Wyeth Pharmaceuticals Company
FDA Application #
NDA018989
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
05-18-1984
Listing Expiration
12-31-2020
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 52904-786-50 identifies a specific commercial package of 50 pouch in 1 case / 2 tablet, coated in 1 pouch of Advil, labeled by Wyeth Pharmaceuticals Company. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Wyeth Pharmaceuticals Company on May 18, 1984. The current certification is valid through December 31, 2020.

How is this Wyeth Pharmaceuticals Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52904078650. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
52904-786-50
11-Digit CMS (5-4-2)
52904-0786-50

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.