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  5. NDC Package Code: 62211-174-99 Magnesium Oxide

NDC Package 62211-174-99 Magnesium Oxide

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 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:
62211-174-99
Package Description:
22200 TABLET in 1 CARTON
Product Code:
62211-174
Proprietary Name:
Magnesium Oxide
Usage Information:
This medication is a mineral supplement used to prevent and treat low amounts of magnesium in the blood. Some brands are also used to treat symptoms of too much stomach acid such as stomach upset, heartburn, and acid indigestion. Magnesium is very important for the normal functioning of cells, nerves, muscles, bones, and the heart. Usually, a well-balanced diet provides normal blood levels of magnesium. However, certain situations cause your body to lose magnesium faster than you can replace it from your diet. These situations include treatment with "water pills" (diuretics such as furosemide, hydrochlorothiazide), a poor diet, alcoholism, or other medical conditions (e.g., severe diarrhea/vomiting, stomach/intestinal absorption problems, poorly controlled diabetes).
11-Digit NDC Billing Format:
62211017499
Labeler Name:
A&z Pharmaceutical, Inc.
Sample Package:
No
FDA Application Number:
part331
Marketing Category:
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date:
12-03-2003
End Marketing Date:
05-05-2015
Listing Expiration Date:
05-05-2015
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.

Frequently Asked Questions

What is NDC 62211-174-99?

The NDC Packaged Code 62211-174-99 is assigned to a package of 22200 tablet in 1 carton of Magnesium Oxide, labeled by A&z Pharmaceutical, Inc.. The product's dosage form is and is administered via form.

Is NDC 62211-174 included in the NDC Directory?

No, Magnesium Oxide with product code 62211-174 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by A&z Pharmaceutical, Inc. on December 03, 2003 and its listing in the NDC Directory is set to expire on May 05, 2015 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 62211-174-99?

The 11-digit format is 62211017499. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-262211-174-995-4-262211-0174-99