NDC Package 68382-337-06 Glipizide

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:
68382-337-06
Package Description:
30 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Code:
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:
68382033706
Labeler Name:
Zydus Pharmaceuticals Usa Inc.
Sample Package:
No
FDA Application Number:
ANDA203499
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
07-25-2018
End Marketing Date:
04-18-2025
Listing Expiration Date:
04-18-2025
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
68382-337-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE
68382-337-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE
68382-337-101000 TABLET, EXTENDED RELEASE in 1 BOTTLE
68382-337-1460 TABLET, EXTENDED RELEASE in 1 BOTTLE
68382-337-1690 TABLET, EXTENDED RELEASE in 1 BOTTLE
68382-337-7710 BLISTER PACK in 1 CARTON / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68382-337-30)

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 68382-337-06?

The NDC Packaged Code 68382-337-06 is assigned to a package of 30 tablet, extended release in 1 bottle of Glipizide, labeled by Zydus Pharmaceuticals Usa Inc.. The product's dosage form is and is administered via form.

Is NDC 68382-337 included in the NDC Directory?

No, Glipizide with product code 68382-337 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Zydus Pharmaceuticals Usa Inc. on July 25, 2018 and its listing in the NDC Directory is set to expire on April 18, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 68382-337-06?

The 11-digit format is 68382033706. 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
5-3-268382-337-065-4-268382-0337-06