Up And Up Acid Reducer
NDC Package 11673-271-39

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 discontinued by the firm.

Up And Up Acid Reducer is a . Marketed by Target Corporation, this product is identified by NDC 11673-271 and is authorized under FDA application ANDA076760.

Identification & Billing

NDC Package Code
11673-271-39
Package Description
1 BOTTLE in 1 CARTON / 30 TABLET in 1 BOTTLE
Product Code
11673-271
11-Digit Billing Format
11673027139

Clinical Specifications

Proprietary Name
Up And Up Acid Reducer Non Prescription Strength
Dosage Form
-

Regulatory & Marketing

Labeler Name
Target Corporation
FDA Application #
ANDA076760
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
07-31-2009
End Marketing Date
01-30-2015
Listing Expiration
01-30-2015
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (11673-271). Click a package code to view its specific billing and regulatory data.

11673-271-27
1 BOTTLE in 1 CARTON / 80 TABLET 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 11673-271-39 identifies a specific commercial package of 1 bottle in 1 carton / 30 tablet in 1 bottle of Up And Up Acid Reducer Non Prescription Strength, labeled by Target Corporation. 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 Target Corporation on July 31, 2009. The current certification is valid through January 30, 2015.

How is this Target Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 11673027139. 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)
11673-271-39
11-Digit CMS (5-4-2)
11673-0271-39

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