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  5. NDC Package Code: 68071-4483-9 Pantoprazole Sodium

NDC Package 68071-4483-9 Pantoprazole Sodium

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
68071-4483-9
Package Description:
90 TABLET, DELAYED RELEASE in 1 BOTTLE
Product Code:
68071-4483
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:
68071448309
NDC to RxNorm Crosswalk:
  • RxCUI: 314200 - pantoprazole sodium 40 MG Delayed Release Oral Tablet
  • RxCUI: 314200 - pantoprazole 40 MG Delayed Release Oral Tablet
  • RxCUI: 314200 - pantoprazole 40 MG (as pantoprazole sodium sesquihydrate 45.1 MG) Delayed Release Oral Tablet
    • Labeler Name:
    Nucare Pharmaceuticals,inc.
    Sample Package:
    No
    Start Marketing Date:
    12-19-2007
    Listing Expiration Date:
    12-31-2022
    Exclude Flag:
    I
    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.

    Frequently Asked Questions

    What is NDC 68071-4483-9?

    The NDC Packaged Code 68071-4483-9 is assigned to a package of 90 tablet, delayed release in 1 bottle of Pantoprazole Sodium, labeled by Nucare Pharmaceuticals,inc.. The product's dosage form is and is administered via form.

    Is NDC 68071-4483 included in the NDC Directory?

    No, Pantoprazole Sodium with product code 68071-4483 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Nucare Pharmaceuticals,inc. on December 19, 2007 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 68071-4483-9?

    The 11-digit format is 68071448309. 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 5-4-1 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
    5-4-168071-4483-95-4-268071-4483-09