Zegerid Otc
NDC Package 82632-101-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Zegerid Otc is for adults 18 years of age and olderthis product is to be used once a day (every 24 hours), every day for 14 daysit may take 1 to 4 days for full effect, although some people get complete relief of symptoms within 24 hours. Marketed by Riley Consumer Care, Llc, this product is identified by NDC 82632-101 and is authorized under FDA application ANDA204923.

Identification & Billing

NDC Package Code
82632-101-01
Package Description
1 BOTTLE in 1 CARTON / 14 CAPSULE in 1 BOTTLE
Product Code
82632-101
11-Digit Billing Format
82632010101
RxNorm Crosswalk
  • RxCUI: 616539 - omeprazole 20 MG / sodium bicarbonate 1100 MG Oral Capsule
  • RxCUI: 616539 - Omeprazole 20 MG / NaHCO3 1100 MG Oral Capsule
  • RxCUI: 646344 - Zegerid 20 MG / 1100 MG Oral Capsule, Reformulated Aug 2006
  • RxCUI: 646344 - omeprazole 20 MG / sodium bicarbonate 1100 MG Oral Capsule [Zegerid Reformulated Aug 2006]
  • RxCUI: 646344 - Omeprazole 20 MG / NaHCO3 1100 MG Oral Capsule [Zegerid Reformulated Aug 2006]

Clinical Specifications

Proprietary Name
Zegerid Otc
Dosage Form
-
Usage Information
For adults 18 years of age and olderthis product is to be used once a day (every 24 hours), every day for 14 daysit may take 1 to 4 days for full effect, although some people get complete relief of symptoms within 24 hours

Regulatory & Marketing

Labeler Name
Riley Consumer Care, Llc
FDA Application #
ANDA204923
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
12-22-2023
Listing Expiration
12-31-2025
Exclude Flag
I
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (82632-101). Click a package code to view its specific billing and regulatory data.

82632-101-03
3 BOTTLE in 1 CARTON / 14 CAPSULE in 1 BOTTLE

* 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 82632-101-01 identifies a specific commercial package of 1 bottle in 1 carton / 14 capsule in 1 bottle of Zegerid Otc, labeled by Riley Consumer Care, Llc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Riley Consumer Care, Llc on December 22, 2023. The current certification is valid through December 31, 2025.

How is this Riley Consumer Care, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82632010101. 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)
82632-101-01
11-Digit CMS (5-4-2)
82632-0101-01

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