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  5. NDC Package Code: 58602-729-62 Acid Reducer

NDC Package 58602-729-62 Acid Reducer

Omeprazole Tablet, Delayed Release Oral - 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:
58602-729-62
Package Description:
3 BOTTLE in 1 CARTON / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
Product Code:
58602-729
Proprietary Name:
Acid Reducer
Non-Proprietary Name:
Omeprazole
Substance Name:
Omeprazole Magnesium
Usage Information:
Ranitidine is known as an H2 blocker. It works by reducing the amount of acid in your stomach. It is used to prevent and treat heartburn and other symptoms caused by too much acid in the stomach (acid indigestion). This drug has been withdrawn from the US market due to problems with safety. A possible cancer-causing impurity has been found in some ranitidine products.
11-Digit NDC Billing Format:
58602072962
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
3 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 402014 - omeprazole 20 MG Delayed Release Oral Tablet
  • RxCUI: 402014 - omeprazole 20 MG (as omeprazole magnesium 20.6 MG) Delayed Release Oral Tablet
Product Type:
Human Otc Drug
Labeler Name:
Aurohealth 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):
OMEPRAZOLE MAGNESIUM 20 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA206877
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
06-06-2018
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
58602-729-011 BLISTER PACK in 1 CARTON / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
58602-729-022 BLISTER PACK in 1 CARTON / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
58602-729-033 BLISTER PACK in 1 CARTON / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
58602-729-051 BOTTLE in 1 CARTON / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
58602-729-612 BOTTLE in 1 CARTON / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
58602-729-652 BLISTER PACK in 1 CARTON / 7 TABLET, DELAYED RELEASE in 1 BLISTER PACK (58602-729-64)

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 58602-729-62?

The NDC Packaged Code 58602-729-62 is assigned to a package of 3 bottle in 1 carton / 14 tablet, delayed release in 1 bottle of Acid Reducer, a human over the counter drug labeled by Aurohealth Llc. The product's dosage form is tablet, delayed release and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 3 billable units per package.

Is NDC 58602-729 included in the NDC Directory?

Yes, Acid Reducer with product code 58602-729 is active and included in the NDC Directory. The product was first marketed by Aurohealth Llc on June 06, 2018 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 NDC billing unit for package 58602-729-62?

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 3.

What is the 11-digit format for NDC 58602-729-62?

The 11-digit format is 58602072962. 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
5-3-258602-729-625-4-258602-0729-62