Equaline Complete Tablet, Chewable
NDC Package 41163-321-63

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

Equaline Complete (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 United Natural Foods, Inc. Dba Unfi, this product is identified by NDC 41163-321 and is authorized under FDA application ANDA077355.

Identification & Billing

NDC Package Code
41163-321-63
Package Description
25 TABLET, CHEWABLE in 1 BOTTLE
Product Code
41163-321
11-Digit Billing Format
41163032163
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
25 EA
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
Equaline Complete Dual Action
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
United Natural Foods, Inc. Dba Unfi
Product Type
Human Otc Drug
FDA Application #
ANDA077355
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
09-02-2008
Listing Expiration
12-31-2027
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (41163-321). Click a package code to view its specific billing and regulatory data.

41163-321-71
50 TABLET, CHEWABLE 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 41163-321-63 identifies a specific commercial package of 25 tablet, chewable in 1 bottle of Equaline Complete Dual Action, a human over the counter drug labeled by United Natural Foods, Inc. Dba Unfi. This product is billed for "EA" each discreet unit and contains an estimated amount of 25 billable units per package. 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 United Natural Foods, Inc. Dba Unfi on September 02, 2008. The current certification is valid through December 31, 2027.

How is this United Natural Foods, Inc. Dba Unfi product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 41163032163. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 25 total billable units per package. 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)
41163-321-63
11-Digit CMS (5-4-2)
41163-0321-63

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