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  5. NDC Package Code: 0008-0607-04 Pantoprazole Sodium Delayed-release

NDC Package 0008-0607-04 Pantoprazole Sodium Delayed-release

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 .

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:
0008-0607-04
Package Description:
100 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product Code:
0008-0607
Proprietary Name:
Pantoprazole Sodium Delayed-release
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:
00008060704
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
100 EA
Labeler Name:
Wyeth Pharmaceuticals Inc., A Subsidiary Of Pfizer Inc.
Sample Package:
No
FDA Application Number:
NDA020987
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
01-31-2008
End Marketing Date:
10-31-2017
Listing Expiration Date:
10-31-2017
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
0008-0607-0190 TABLET, DELAYED RELEASE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 0008-0607-04?

The NDC Packaged Code 0008-0607-04 is assigned to a package of 100 blister pack in 1 carton / 1 tablet, delayed release in 1 blister pack of Pantoprazole Sodium Delayed-release, labeled by Wyeth Pharmaceuticals Inc., A Subsidiary Of Pfizer Inc.. The product's dosage form is and is administered via form.

Is NDC 0008-0607 included in the NDC Directory?

The product was first marketed by Wyeth Pharmaceuticals Inc., A Subsidiary Of Pfizer Inc. on January 31, 2008 and its listing in the NDC Directory is set to expire on October 31, 2017 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 0008-0607-04?

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 0008-0607-04?

The 11-digit format is 00008060704. 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 4-4-2 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
4-4-20008-0607-045-4-200008-0607-04