1. Home
  2. Labeler Index
  3. Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc.
  4. 0008-0923
  5. NDC Package Code: 0008-0923-51 Protonix I.v.

NDC Package 0008-0923-51 Protonix I.v.

Pantoprazole Sodium Injection, Powder, For Solution Intravenous - 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:
0008-0923-51
Package Description:
1 VIAL in 1 CARTON / 10 mL in 1 VIAL
Product Code:
0008-0923
Proprietary Name:
Protonix I.v.
Non-Proprietary Name:
Pantoprazole Sodium
Substance 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:
00008092351
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 283669 - pantoprazole 40 MG Injection
  • RxCUI: 283669 - pantoprazole (as sodium) 40 MG Injection
  • RxCUI: 885257 - PROTONIX 40 MG Injection
  • RxCUI: 885257 - pantoprazole 40 MG Injection [Protonix]
  • RxCUI: 885257 - Protonix 40 MG Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc.
    Dosage Form:
    Injection, Powder, For Solution - A sterile preparation intended for reconstitution to form a solution for parenteral use.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • PANTOPRAZOLE SODIUM 40 mg/10mL
    • Pharmacologic Class(es):
  • Proton Pump Inhibitor - [EPC] (Established Pharmacologic Class)
  • Proton Pump Inhibitors - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    NDA020988
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    05-01-2001
    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
    0008-0923-5510 CARTON in 1 PACKAGE / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL
    0008-0923-6025 CARTON in 1 PACKAGE / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0008-0923-51?

    The NDC Packaged Code 0008-0923-51 is assigned to a package of 1 vial in 1 carton / 10 ml in 1 vial of Protonix I.v., a human prescription drug labeled by Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc.. The product's dosage form is injection, powder, for solution and is administered via intravenous form.

    Is NDC 0008-0923 included in the NDC Directory?

    Yes, Protonix I.v. with product code 0008-0923 is active and included in the NDC Directory. The product was first marketed by Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc. on May 01, 2001 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 0008-0923-51?

    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 1.

    What is the 11-digit format for NDC 0008-0923-51?

    The 11-digit format is 00008092351. 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
    4-4-20008-0923-515-4-200008-0923-51