Up And Up Dual Action Acid Reducer Antacid Tablet, Chewable
NDC Package 82442-321-71

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

Package Information

Up And Up Dual Action Acid Reducer Antacid (famotidine, calcium carbonate and magnesium hydroxide) tablets is •adults and children 12 years and over:•do not swallow tablet whole: chew completely•to relieve symptoms, chew 1 tablet before swallowing•do not use more than 2 chewable tablets in 24 hours•children under 12 years: ask a doctor. This formulation utilizes a tablet, chewable delivery system. Marketed by Target Corporation, this product is identified by NDC 82442-321 and is authorized under FDA application ANDA077355.

Identification & Billing

NDC Package Code
82442-321-71
Package Description
50 TABLET, CHEWABLE in 1 BOTTLE
Product Code
82442-321
11-Digit Billing Format
82442032171
RxNorm Crosswalk
  • RxCUI: 283641 - famotidine 10 MG / calcium carbonate 800 MG / magnesium hydroxide 165 MG Chewable Tablet
  • RxCUI: 283641 - calcium carbonate 800 MG / famotidine 10 MG / magnesium hydroxide 165 MG Chewable Tablet
  • RxCUI: 283641 - calcium carbonate 800 MG / famotidine 10 MG / milk of magnesia 165 MG Chewable Tablet

Clinical Specifications

Proprietary Name
Up And Up Dual Action Acid Reducer Antacid
Non-Proprietary Name
Famotidine, Calcium Carbonate And Magnesium Hydroxide
Substance Name
Calcium Carbonate; Famotidine; Magnesium Hydroxide
Dosage Form
Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
•adults and children 12 years and over:•do not swallow tablet whole: chew completely•to relieve symptoms, chew 1 tablet before swallowing•do not use more than 2 chewable tablets in 24 hours•children under 12 years: ask a doctor

Regulatory & Marketing

Labeler Name
Target Corporation
Product Type
Human Otc Drug
FDA Application #
ANDA077355
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
01-08-2025
Listing Expiration
12-31-2026
Exclude Flag
N
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 82442-321-71 identifies a specific commercial package of 50 tablet, chewable in 1 bottle of Up And Up Dual Action Acid Reducer Antacid, a human over the counter drug labeled by Target Corporation. This tablet, chewable is formulated for oral use and contains calcium carbonate; famotidine; magnesium hydroxide as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Target Corporation on January 08, 2025. The current certification is valid through December 31, 2026.

How is this Target Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82442032171. 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)
82442-321-71
11-Digit CMS (5-4-2)
82442-0321-71

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