1. Home
  2. Labeler Index
  3. Abbvie Inc.
  4. 0074-3161
  5. NDC Package Code: 0074-3161-90 Trilipix

NDC Package 0074-3161-90 Trilipix

View Billable Units, 11-Digit Format, RxNorm

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 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:
0074-3161-90
Package Description:
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product Code:
0074-3161
Proprietary Name:
Trilipix
Usage Information:
Fenofibric acid is used along with a proper diet to help lower "bad" cholesterol and fats (such as LDL, triglycerides) and raise "good" cholesterol (HDL) in the blood. It works by increasing the natural substance (enzyme) that breaks down fats in the blood. Fenofibric acid belongs to a group of drugs known as "fibrates." Lowering triglycerides in people with very high triglyceride blood levels may decrease the risk of pancreas disease (pancreatitis). However, fenofibric acid might not lower your risk of a heart attack or stroke. Talk to your doctor about the risks and benefits of fenofibric acid. In addition to eating a proper diet (such as a low-cholesterol/low-fat diet), other lifestyle changes that may help this medication work better include exercising, losing weight if overweight, and stopping smoking. Consult your doctor for more details.
11-Digit NDC Billing Format:
00074316190
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:
Abbvie Inc.
Sample Package:
No
FDA Application Number:
NDA022224
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
09-12-2016
End Marketing Date:
04-30-2025
Listing Expiration Date:
04-30-2025
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.

Frequently Asked Questions

What is NDC 0074-3161-90?

The NDC Packaged Code 0074-3161-90 is assigned to a package of 90 capsule, delayed release in 1 bottle of Trilipix, labeled by Abbvie Inc.. The product's dosage form is and is administered via form.

Is NDC 0074-3161 included in the NDC Directory?

No, Trilipix with product code 0074-3161 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Abbvie Inc. on September 12, 2016 and its listing in the NDC Directory is set to expire on April 30, 2025 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 0074-3161-90?

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 0074-3161-90?

The 11-digit format is 00074316190. 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 4-4-2 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
4-4-20074-3161-905-4-200074-3161-90