Acid Reducer
NDC Package 37808-710-02

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
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.

Acid Reducer is ranitidine is known as an H2 blocker. Marketed by H E B, this product is identified by NDC 37808-710 and is authorized under FDA application ANDA091429.

Identification & Billing

NDC Package Code
37808-710-02
Package Description
1 BOTTLE in 1 CARTON / 24 TABLET, FILM COATED in 1 BOTTLE
Product Code
37808-710
11-Digit Billing Format
37808071002

Clinical Specifications

Proprietary Name
Acid Reducer
Dosage Form
-
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 This drug has been withdrawn from the US market due to problems with safety.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.

Regulatory & Marketing

Labeler Name
H E B
FDA Application #
ANDA091429
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
11-25-2015
End Marketing Date
06-30-2021
Listing Expiration
06-30-2021
Exclude Flag
D
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 37808-710-02 identifies a specific commercial package of 1 bottle in 1 carton / 24 tablet, film coated in 1 bottle of Acid Reducer, labeled by H E B. 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 H E B on November 25, 2015. The current certification is valid through June 30, 2021.

What are the primary indications for this medication?

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.

How is this H E B product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 37808071002. 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)
37808-710-02
11-Digit CMS (5-4-2)
37808-0710-02

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