NDC Package 50742-151-90 Pantoprazole Sodium

View Billable Units, 11-Digit Format, RxNorm

Package Information
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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:

50742-151-90

Package Description:

90 TABLET, DELAYED RELEASE in 1 BOTTLE

Product Code:

50742-151

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:

50742015190

Labeler Name:

Ingenus Pharmaceuticals, Llc

Sample Package:

FDA Application Number:

ANDA211368

Marketing Category:

ANDA - A product marketed under an approved Abbreviated New Drug Application.

Start Marketing Date:

03-11-2019

End Marketing Date:

01-31-2024

Listing Expiration Date:

01-31-2024

Exclude Flag:

Code Structure:

50742 - Ingenus Pharmaceuticals, Llc
- 50742-151 - Pantoprazole Sodium
  - 50742-151-90 - 90 TABLET, DELAYED 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
50742-151-10	1000 TABLET, DELAYED RELEASE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 50742-151-90?

The NDC Packaged Code 50742-151-90 is assigned to a package of 90 tablet, delayed release in 1 bottle of Pantoprazole Sodium, labeled by Ingenus Pharmaceuticals, Llc. The product's dosage form is and is administered via form.

Is NDC 50742-151 included in the NDC Directory?

No, Pantoprazole Sodium with product code 50742-151 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Ingenus Pharmaceuticals, Llc on March 11, 2019 and its listing in the NDC Directory is set to expire on January 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 50742-151-90?

The 11-digit format is 50742015190. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	50742-151-90	5-4-2	50742-0151-90

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