Dual Action
NDC Package 56062-321-63

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.

Dual Action is a . Marketed by Publix Super Markets Inc, this product is identified by NDC 56062-321 and is authorized under FDA application ANDA077355.

Identification & Billing

NDC Package Code
56062-321-63
Package Description
25 TABLET, CHEWABLE in 1 BOTTLE
Product Code
11-Digit Billing Format
56062032163
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
25 EA

Clinical Specifications

Proprietary Name
Dual Action
Dosage Form
-

Regulatory & Marketing

Labeler Name
Publix Super Markets Inc
FDA Application #
ANDA077355
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
12-05-2008
End Marketing Date
02-29-2020
Listing Expiration
02-29-2020
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 (56062-321). Click a package code to view its specific billing and regulatory data.

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 56062-321-63 identifies a specific commercial package of 25 tablet, chewable in 1 bottle of Dual Action, labeled by Publix Super Markets Inc. This product is billed for "EA" each discreet unit and contains an estimated amount of 25 billable units per package. 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 Publix Super Markets Inc on December 05, 2008. The current certification is valid through February 29, 2020.

How is this Publix Super Markets Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 56062032163. 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)
56062-321-63
11-Digit CMS (5-4-2)
56062-0321-63

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