NDC Package 68788-7230-9 Glipizide

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:

68788-7230-9

Package Description:

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

Product Code:

68788-7230

Proprietary Name:

Glipizide

Usage Information:

Glipizide is used with a proper diet and exercise program to control high blood sugar in people with type 2 diabetes. It may also be used with other diabetes medications. Controlling high blood sugar helps prevent kidney damage, blindness, nerve problems, loss of limbs, and sexual function problems. Proper control of diabetes may also lessen your risk of a heart attack or stroke. Glipizide belongs to the class of drugs known as sulfonylureas. It lowers blood sugar by causing the release of your body's natural insulin.

11-Digit NDC Billing Format:

68788723009

NDC to RxNorm Crosswalk:

RxCUI: 315107 - glipiZIDE 10 MG 24HR Extended Release Oral Tablet

RxCUI: 315107 - 24 HR glipizide 10 MG Extended Release Oral Tablet

RxCUI: 315107 - glipizide ER 10 MG 24 HR Extended Release Oral Tablet

RxCUI: 315107 - glipizide XL 10 MG 24 HR Extended Release Oral Tablet

Labeler Name:

Preferred Pharmaceuticals Inc.

Sample Package:

Start Marketing Date:

08-06-2018

Listing Expiration Date:

12-31-2021

Exclude Flag:

Code Structure:

68788 - Preferred Pharmaceuticals Inc.
- 68788-7230 - Glipizide
  - 68788-7230-9 - 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

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
68788-7230-1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
68788-7230-3	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
68788-7230-6	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 68788-7230-9?

The NDC Packaged Code 68788-7230-9 is assigned to a package of 90 tablet, film coated, extended release in 1 bottle of Glipizide, labeled by Preferred Pharmaceuticals Inc.. The product's dosage form is and is administered via form.

Is NDC 68788-7230 included in the NDC Directory?

No, Glipizide with product code 68788-7230 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Preferred Pharmaceuticals Inc. on August 06, 2018 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 68788-7230-9?

The 11-digit format is 68788723009. 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 5-4-1 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
5-4-1	68788-7230-9	5-4-2	68788-7230-09

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