1. Home
  2. Labeler Index
  3. Zydus Pharmaceuticals Usa Inc.
  4. 68382-185
  5. NDC Package Code: 68382-185-01 Glipizide And Metformin Hydrochloride

NDC Package 68382-185-01 Glipizide And Metformin Hydrochloride

Tablet, Film Coated 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:
68382-185-01
Package Description:
100 TABLET, FILM COATED in 1 BOTTLE
Product Code:
68382-185
Proprietary Name:
Glipizide And Metformin Hydrochloride
Non-Proprietary Name:
Glipizide And Metformin Hydrochloride
Substance Name:
Glipizide; Metformin Hydrochloride
Usage Information:
Glipizide and metformin hydrochloride tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.
11-Digit NDC Billing Format:
68382018501
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
100 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 861731 - glipiZIDE 2.5 MG / metFORMIN HCl 250 MG Oral Tablet
  • RxCUI: 861731 - glipizide 2.5 MG / metformin hydrochloride 250 MG Oral Tablet
  • RxCUI: 861736 - glipiZIDE 2.5 MG / metFORMIN HCl 500 MG Oral Tablet
  • RxCUI: 861736 - glipizide 2.5 MG / metformin hydrochloride 500 MG Oral Tablet
  • RxCUI: 861740 - glipiZIDE 5 MG / metFORMIN HCl 500 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Zydus Pharmaceuticals Usa Inc.
    Dosage Form:
    Tablet, Film Coated - 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.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • GLIPIZIDE 2.5 mg/1
  • METFORMIN HYDROCHLORIDE 500 mg/1
    • Pharmacologic Class(es):
  • Biguanide - [EPC] (Established Pharmacologic Class)
  • Biguanides - [CS]
  • Sulfonylurea Compounds - [CS]
  • Sulfonylurea - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA078905
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    05-05-2016
    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
    68382-185-101000 TABLET, FILM COATED in 1 BOTTLE
    68382-185-1690 TABLET, FILM COATED in 1 BOTTLE
    68382-185-7710 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-185-30)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 68382-185-01?

    The NDC Packaged Code 68382-185-01 is assigned to a package of 100 tablet, film coated in 1 bottle of Glipizide And Metformin Hydrochloride, a human prescription drug labeled by Zydus Pharmaceuticals Usa Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 68382-185 included in the NDC Directory?

    Yes, Glipizide And Metformin Hydrochloride with product code 68382-185 is active and included in the NDC Directory. The product was first marketed by Zydus Pharmaceuticals Usa Inc. on May 05, 2016 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 68382-185-01?

    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 100.

    What is the 11-digit format for NDC 68382-185-01?

    The 11-digit format is 68382018501. 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
    5-3-268382-185-015-4-268382-0185-01