Aptrizine
NDC Package 46084-012-15

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 inactivated by the FDA.

Aptrizine is temporarily relieves these symptoms due to hay fever or other upper respiratory allergies, runny nose, sneezing, itchy, watery eyes, itching of the nose or throat. Marketed by A P J Laboratories Limited, this product is identified by NDC 46084-012 and is authorized under FDA application ANDA019835.

Identification & Billing

NDC Package Code
46084-012-15
Package Description
120 TABLET in 1 BLISTER PACK
Product Code
46084-012
11-Digit Billing Format
46084001215
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Aptrizine 24-hour All Day Allergy
Dosage Form
-
Usage Information
Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies, runny nose, sneezing, itchy, watery eyes, itching of the nose or throat.

Regulatory & Marketing

Labeler Name
A P J Laboratories Limited
FDA Application #
ANDA019835
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
02-21-2013
Listing Expiration
12-31-2017
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (46084-012). Click a package code to view its specific billing and regulatory data.

46084-012-11
15 TABLET in 1 BLISTER PACK
46084-012-12
30 TABLET in 1 BLISTER PACK
46084-012-13
45 TABLET in 1 BLISTER PACK
46084-012-14
60 TABLET in 1 BLISTER PACK

* 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 46084-012-15 identifies a specific commercial package of 120 tablet in 1 blister pack of Aptrizine 24-hour All Day Allergy, labeled by A P J Laboratories Limited. 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 A P J Laboratories Limited on February 21, 2013. The current certification is valid through December 31, 2017.

How is this A P J Laboratories Limited product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 46084001215. 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)
46084-012-15
11-Digit CMS (5-4-2)
46084-0012-15

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