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  5. NDC Package Code: 64980-280-05 Glipizide

NDC Package 64980-280-05 Glipizide

Tablet, Film Coated, Extended Release Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
64980-280-05
Package Description:
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Code:
64980-280
Proprietary Name:
Glipizide
Non-Proprietary Name:
Glipizide
Substance 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:
64980028005
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
500 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 310489 - glipiZIDE 2.5 MG 24HR Extended Release Oral Tablet
  • RxCUI: 310489 - 24 HR glipizide 2.5 MG Extended Release Oral Tablet
  • RxCUI: 310489 - glipizide ER 2.5 MG 24 HR Extended Release Oral Tablet
  • RxCUI: 310489 - glipizide XL 2.5 MG 24 HR Extended Release Oral Tablet
  • RxCUI: 314006 - glipiZIDE 5 MG 24HR Extended Release Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Rising Pharmaceuticals, Inc.
    Dosage Form:
    Tablet, Film Coated, Extended Release - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer; the tablet is formulated in such manner as to make the contained medicament available over an extended period of time following ingestion.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • GLIPIZIDE 5 mg/1
    • Pharmacologic Class(es):
  • Sulfonylurea Compounds - [CS]
  • Sulfonylurea - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA204720
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-24-2017
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    64980-280-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
    64980-280-101000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 64980-280-05?

    The NDC Packaged Code 64980-280-05 is assigned to a package of 500 tablet, film coated, extended release in 1 bottle, plastic of Glipizide, a human prescription drug labeled by Rising Pharmaceuticals, Inc.. The product's dosage form is tablet, film coated, extended release and is administered via oral form.

    Is NDC 64980-280 included in the NDC Directory?

    Yes, Glipizide with product code 64980-280 is active and included in the NDC Directory. The product was first marketed by Rising Pharmaceuticals, Inc. on April 24, 2017 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 NDC billing unit for package 64980-280-05?

    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 500.

    What is the 11-digit format for NDC 64980-280-05?

    The 11-digit format is 64980028005. 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
    5-3-264980-280-055-4-264980-0280-05