NDC Package 55154-7634-0 Pantoprazole Sodium

Tablet, Delayed Release Oral - View Billable Units, 11-Digit Format, RxNorm

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:
55154-7634-0
Package Description:
10 BLISTER PACK in 1 BAG / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product Code:
Proprietary Name:
Pantoprazole Sodium
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:
55154763400
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
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Cardinal Health 107, Llc
    Dosage Form:
    Tablet, Delayed Release - A solid dosage form which releases a drug (or drugs) at a time other than promptly after administration. Enteric-coated articles are delayed release dosage forms.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA090074
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    06-01-2015
    Listing Expiration Date:
    12-31-2025
    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.

    Frequently Asked Questions

    What is NDC 55154-7634-0?

    The NDC Packaged Code 55154-7634-0 is assigned to a package of 10 blister pack in 1 bag / 1 tablet, delayed release in 1 blister pack of Pantoprazole Sodium, a human prescription drug labeled by Cardinal Health 107, Llc. The product's dosage form is tablet, delayed release and is administered via oral form.

    Is NDC 55154-7634 included in the NDC Directory?

    Yes, Pantoprazole Sodium with product code 55154-7634 is active and included in the NDC Directory. The product was first marketed by Cardinal Health 107, Llc on June 01, 2015 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 55154-7634-0?

    The 11-digit format is 55154763400. 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
    5-4-155154-7634-05-4-255154-7634-00