NDC Package 75987-010-03 Duexis

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
75987-010-03
Package Description:
90 TABLET, COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Duexis
Usage Information:
This combination medication is used to relieve pain from rheumatoid arthritis and osteoarthritis while decreasing the risk of developing an ulcer from ibuprofen use. It contains ibuprofen and famotidine. Ibuprofen is a nonsteroidal anti-inflammatory drug (NSAID) that works by blocking your body's production of certain natural substances that cause inflammation. This helps to decrease swelling and pain. Famotidine is an H2 blocker that works by reducing the amount of acid in your stomach. This helps prevent ulcers. Ask your doctor about non-drug treatments and/or using other medications to treat your pain. See also Warning section.
11-Digit NDC Billing Format:
75987001003
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
90 EA
Labeler Name:
Horizon Therapeutics Usa, Inc.
Sample Package:
No
FDA Application Number:
NDA022519
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
12-05-2011
End Marketing Date:
08-31-2025
Listing Expiration Date:
08-31-2025
Exclude Flag:
D
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
75987-010-729 BLISTER PACK in 1 CARTON / 3 TABLET, COATED in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 75987-010-03?

The NDC Packaged Code 75987-010-03 is assigned to a package of 90 tablet, coated in 1 bottle of Duexis, labeled by Horizon Therapeutics Usa, Inc.. The product's dosage form is and is administered via form.This product is billed for "EA" each discreet unit and contains an estimated amount of 90 billable units per package.

Is NDC 75987-010 included in the NDC Directory?

No, Duexis with product code 75987-010 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Horizon Therapeutics Usa, Inc. on December 05, 2011 and its listing in the NDC Directory is set to expire on August 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 75987-010-03?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 90.

What is the 11-digit format for NDC 75987-010-03?

The 11-digit format is 75987001003. 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
5-3-275987-010-035-4-275987-0010-03