Up And Up Ultra Strength Antacid 1000
NDC Package 82442-101-72

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 inactivated by the FDA.

Up And Up Ultra Strength Antacid 1000 is • adults and children 12 years of age and over: chew 2-3 tablets completely as symptoms occur, or as directed by a doctor. Marketed by Target Corporation, this product is identified by NDC 82442-101 and is authorized under FDA application part331.

Identification & Billing

NDC Package Code
82442-101-72
Package Description
72 TABLET, CHEWABLE in 1 BOTTLE
Product Code
82442-101
11-Digit Billing Format
82442010172
RxNorm Crosswalk
  • RxCUI: 308892 - calcium carbonate 1000 MG (Ca 400 MG) Chewable Tablet
  • RxCUI: 308892 - calcium carbonate 1000 MG Chewable Tablet
  • RxCUI: 308892 - calcium carbonate 1000 MG (calcium 400 MG) Chewable Tablet

Clinical Specifications

Proprietary Name
Up And Up Ultra Strength Antacid 1000
Dosage Form
-
Usage Information
• adults and children 12 years of age and over: chew 2-3 tablets completely as symptoms occur, or as directed by a doctor. Do not swallow tablets whole.• do not take for symptoms that persist for more than 2 weeks unless advised by a doctor

Regulatory & Marketing

Labeler Name
Target Corporation
FDA Application #
part331
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
04-07-2023
Listing Expiration
12-31-2024
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 82442-101-72 identifies a specific commercial package of 72 tablet, chewable in 1 bottle of Up And Up Ultra Strength Antacid 1000, 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 April 07, 2023. The current certification is valid through December 31, 2024.

How is this Target Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82442010172. 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)
82442-101-72
11-Digit CMS (5-4-2)
82442-0101-72

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