Acid Reducer
NDC Package 41268-141-65

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

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 Hannaford Brothers Company, this product is identified by NDC 41268-141 and is authorized under FDA application ANDA075400.

Identification & Billing

NDC Package Code
41268-141-65
Package Description
3 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
Product Code
11-Digit Billing Format
41268014165

Clinical Specifications

Proprietary Name
Acid Reducer Original Strength
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 This drug has been withdrawn from the US market due to problems with safety.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
Hannaford Brothers Company
FDA Application #
ANDA075400
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
02-03-2010
End Marketing Date
04-10-2012
Listing Expiration
04-10-2012
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 41268-141-65 identifies a specific commercial package of 3 blister pack in 1 carton / 10 tablet in 1 blister pack of Acid Reducer Original Strength, labeled by Hannaford Brothers Company. 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 Hannaford Brothers Company on February 03, 2010. The current certification is valid through April 10, 2012.

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 Hannaford Brothers Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 41268014165. 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)
41268-141-65
11-Digit CMS (5-4-2)
41268-0141-65

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