NDC Package 52725-495-90 Fenoglide

View Billable Units, 11-Digit Format, RxNorm

Package Information
Other Packages
Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:

52725-495-90

Package Description:

90 TABLET in 1 BOTTLE, PLASTIC

Product Code:

52725-495

Proprietary Name:

Fenoglide

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:

52725049590

NDC to RxNorm Crosswalk:

RxCUI: 749802 - fenofibrate 120 MG Oral Tablet

RxCUI: 749804 - fenofibrate 40 MG Oral Tablet

RxCUI: 763250 - Fenoglide 120 MG Oral Tablet

RxCUI: 763250 - fenofibrate 120 MG Oral Tablet [Fenoglide]

RxCUI: 763252 - Fenoglide 40 MG Oral Tablet

Labeler Name:

Shore Therapeutics, Inc

Sample Package:

Start Marketing Date:

11-18-2010

Listing Expiration Date:

12-31-2018

Exclude Flag:

Code Structure:

52725 - Shore Therapeutics, Inc
- 52725-495 - Fenoglide
  - 52725-495-90 - 90 TABLET in 1 BOTTLE, PLASTIC

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 Code	Package Description
52725-495-07	6 BOTTLE, PLASTIC in 1 BOX / 7 TABLET in 1 BOTTLE, PLASTIC

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 52725-495-90?

The NDC Packaged Code 52725-495-90 is assigned to a package of 90 tablet in 1 bottle, plastic of Fenoglide, labeled by Shore Therapeutics, Inc. The product's dosage form is and is administered via form.

Is NDC 52725-495 included in the NDC Directory?

No, Fenoglide with product code 52725-495 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Shore Therapeutics, Inc on November 18, 2010 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 52725-495-90?

The 11-digit format is 52725049590. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	52725-495-90	5-4-2	52725-0495-90

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