NDC Package 68084-715-32 Fenofibric Acid Delayed-release

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:
68084-715-32
Package Description:
20 BLISTER PACK in 1 BOX, UNIT-DOSE / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (68084-715-33)
Product Code:
Proprietary Name:
Fenofibric Acid Delayed-release
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:
68084071532
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
20 EA
Labeler Name:
American Health Packaging
Sample Package:
No
FDA Application Number:
ANDA201573
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
02-15-2015
End Marketing Date:
09-30-2016
Listing Expiration Date:
09-30-2016
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 68084-715-32?

The NDC Packaged Code 68084-715-32 is assigned to a package of 20 blister pack in 1 box, unit-dose / 1 capsule, delayed release in 1 blister pack (68084-715-33) of Fenofibric Acid Delayed-release, labeled by American Health Packaging. The product's dosage form is and is administered via form.

Is NDC 68084-715 included in the NDC Directory?

No, Fenofibric Acid Delayed-release with product code 68084-715 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by American Health Packaging on February 15, 2015 and its listing in the NDC Directory is set to expire on September 30, 2016 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 68084-715-32?

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 20.

What is the 11-digit format for NDC 68084-715-32?

The 11-digit format is 68084071532. 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
5-3-268084-715-325-4-268084-0715-32