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  5. NDC Package Code: 62175-180-43 Pantoprazole Sodium

NDC Package 62175-180-43 Pantoprazole Sodium

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

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

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:
62175-180-43
Package Description:
1000 TABLET, DELAYED RELEASE in 1 BOTTLE
Product Code:
62175-180
Proprietary Name:
Pantoprazole Sodium
Usage Information:
Pantoprazole is used to treat certain stomach and esophagus problems (such as acid reflux). It works by decreasing the amount of acid your stomach makes. This medication relieves symptoms such as heartburn, difficulty swallowing, and persistent cough. It helps heal acid damage to the stomach and esophagus, helps prevent ulcers, and may help prevent cancer of the esophagus. Pantoprazole belongs to a class of drugs known as proton pump inhibitors (PPIs).
11-Digit NDC Billing Format:
62175018043
NDC to RxNorm Crosswalk:
  • RxCUI: 251872 - pantoprazole sodium 20 MG Delayed Release Oral Tablet
  • RxCUI: 251872 - pantoprazole 20 MG Delayed Release Oral Tablet
  • RxCUI: 251872 - pantoprazole 20 MG (as pantoprazole sodium sesquihydrate 22.56 MG) Delayed Release Oral Tablet
  • RxCUI: 314200 - pantoprazole sodium 40 MG Delayed Release Oral Tablet
  • RxCUI: 314200 - pantoprazole 40 MG Delayed Release Oral Tablet
Labeler Name:
Lannett Company, Inc.
Sample Package:
No
FDA Application Number:
ANDA078281
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
01-20-2011
End Marketing Date:
03-31-2023
Listing Expiration Date:
03-31-2023
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
62175-180-4690 TABLET, DELAYED RELEASE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 62175-180-43?

The NDC Packaged Code 62175-180-43 is assigned to a package of 1000 tablet, delayed release in 1 bottle of Pantoprazole Sodium, labeled by Lannett Company, Inc.. The product's dosage form is and is administered via form.

Is NDC 62175-180 included in the NDC Directory?

No, Pantoprazole Sodium with product code 62175-180 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Lannett Company, Inc. on January 20, 2011 and its listing in the NDC Directory is set to expire on March 31, 2023 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 62175-180-43?

The 11-digit format is 62175018043. 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
5-3-262175-180-435-4-262175-0180-43