24 Hour Omeprazole Tablet, Delayed Release
NDC Package 85828-731-45

11-digit billing NDC: 85828073145

Package Information

24 Hour Omeprazole (omeprazole 20 mg) tablets is usestreats frequent heartburn (occurs 2 or moredays a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect. This formulation utilizes a tablet, delayed release delivery system. Marketed by Grocery Outlet, Inc., this product is identified by NDC 85828-731 and is authorized under FDA application ANDA218829.

Identification & Billing

NDC Package Code
85828-731-45
Package Description
1 BOTTLE in 1 CARTON / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
Product Code
11-Digit Billing Format
85828073145
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

Clinical Specifications

Proprietary Name
24 Hour Omeprazole
Non-Proprietary Name
Omeprazole 20 Mg
Substance Name
Omeprazole Magnesium
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
Usestreats frequent heartburn (occurs 2 or moredays a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Regulatory & Marketing

Labeler Name
Grocery Outlet, Inc.
Product Type
Human Otc Drug
FDA Application #
ANDA218829
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
03-25-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 85828-731-45 identifies a specific commercial package of 1 bottle in 1 carton / 14 tablet, delayed release in 1 bottle of 24 Hour Omeprazole, a human over the counter drug labeled by Grocery Outlet, Inc.. This tablet, delayed release is formulated for oral use and contains omeprazole magnesium as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Grocery Outlet, Inc. on March 25, 2026. The current certification is valid through December 31, 2027.

How is this Grocery Outlet, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 85828073145. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
85828-731-45
11-Digit CMS (5-4-2)
85828-0731-45

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.