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  5. NDC Package Code: 75987-010-03 Duexis

NDC Package 75987-010-03 Duexis

Ibuprofen And Famotidine Tablet, Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
75987-010-03
Package Description:
90 TABLET, COATED in 1 BOTTLE
Product Code:
75987-010
Proprietary Name:
Duexis
Non-Proprietary Name:
Ibuprofen And Famotidine
Substance Name:
Famotidine; Ibuprofen
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
NDC to RxNorm Crosswalk:
  • RxCUI: 1100066 - ibuprofen 800 MG / famotidine 26.6 MG Oral Tablet
  • RxCUI: 1100066 - famotidine 26.6 MG / ibuprofen 800 MG Oral Tablet
  • RxCUI: 1100070 - DUEXIS 800 MG / 26.6 MG Oral Tablet
  • RxCUI: 1100070 - famotidine 26.6 MG / ibuprofen 800 MG Oral Tablet [Duexis]
  • RxCUI: 1100070 - Duexis (famotidine 26.6 MG / ibuprofen 800 MG) Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Horizon Therapeutics Usa, Inc.
    Dosage Form:
    Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • FAMOTIDINE 26.6 mg/1
  • IBUPROFEN 800 mg/1
    • Pharmacologic Class(es):
  • Anti-Inflammatory Agents, Non-Steroidal - [CS]
  • Cyclooxygenase Inhibitors - [MoA] (Mechanism of Action)
  • Histamine H2 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Histamine-2 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
  • Nonsteroidal Anti-inflammatory Drug - [EPC] (Established Pharmacologic Class)
    • 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
    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
    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, a human prescription drug labeled by Horizon Therapeutics Usa, Inc.. The product's dosage form is tablet, coated and is administered via oral form.

    Is NDC 75987-010 included in the NDC Directory?

    Yes, Duexis with product code 75987-010 is active and included in the NDC Directory. The product was first marketed by Horizon Therapeutics Usa, Inc. on December 05, 2011.

    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