NDC Package 0074-3189-90 Tricor

Fenofibrate Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

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:
0074-3189-90
Package Description:
90 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Tricor
Non-Proprietary Name:
Fenofibrate
Substance Name:
Fenofibrate
Usage Information:
Fenofibrate 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. Fenofibrate 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, fenofibrate might not lower your risk of a heart attack or stroke. Talk to your doctor about the risks and benefits of fenofibrate. 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:
00074318990
NDC to RxNorm Crosswalk:
  • RxCUI: 477560 - fenofibrate 145 MG Oral Tablet
  • RxCUI: 477562 - fenofibrate 48 MG Oral Tablet
  • RxCUI: 540281 - TriCor 145 MG Oral Tablet
  • RxCUI: 540281 - fenofibrate 145 MG Oral Tablet [Tricor]
  • RxCUI: 540281 - Tricor 145 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Abbvie 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:
    NDA021656
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    02-05-2016
    Listing Expiration Date:
    12-31-2024
    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.

    Frequently Asked Questions

    What is NDC 0074-3189-90?

    The NDC Packaged Code 0074-3189-90 is assigned to a package of 90 tablet in 1 bottle of Tricor, a human prescription drug labeled by Abbvie Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 0074-3189 included in the NDC Directory?

    Yes, Tricor with product code 0074-3189 is active and included in the NDC Directory. The product was first marketed by Abbvie Inc. on February 05, 2016 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 0074-3189-90?

    The 11-digit format is 00074318990. 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
    4-4-20074-3189-905-4-200074-3189-90