Fexofenadine Hcl
NDC Package 63868-024-15

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 discontinued by the firm.

Fexofenadine Hcl is fexofenadine is an antihistamine used to relieve allergy symptoms such as watery eyes, runny nose, itching eyes/nose, sneezing, hives, and itching. Marketed by Quality Choice (chain Drug Marketing Association), this product is identified by NDC 63868-024 and is authorized under FDA application ANDA079112.

Identification & Billing

NDC Package Code
63868-024-15
Package Description
1 BLISTER PACK in 1 CARTON / 15 TABLET in 1 BLISTER PACK
Product Code
63868-024
11-Digit Billing Format
63868002415

Clinical Specifications

Proprietary Name
Fexofenadine Hcl
Dosage Form
-
Usage Information
Fexofenadine is an antihistamine used to relieve allergy symptoms such as watery eyes, runny nose, itching eyes/nose, sneezing, hives, and itching. It works by blocking a certain natural substance (histamine) that your body makes during an allergic reaction.

Regulatory & Marketing

Labeler Name
Quality Choice (chain Drug Marketing Association)
FDA Application #
ANDA079112
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
08-27-2012
End Marketing Date
12-01-2017
Listing Expiration
12-01-2017
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 (63868-024). Click a package code to view its specific billing and regulatory data.

63868-024-30
1 BOTTLE in 1 BOX / 30 TABLET 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 63868-024-15 identifies a specific commercial package of 1 blister pack in 1 carton / 15 tablet in 1 blister pack of Fexofenadine Hcl, labeled by Quality Choice (chain Drug Marketing Association). 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 Quality Choice (chain Drug Marketing Association) on August 27, 2012. The current certification is valid through December 01, 2017.

What are the primary indications for this medication?

Fexofenadine is an antihistamine used to relieve allergy symptoms such as watery eyes, runny nose, itching eyes/nose, sneezing, hives, and itching. It works by blocking a certain natural substance (histamine) that your body makes during an allergic reaction.

How is this Quality Choice (chain Drug Marketing Association) product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 63868002415. 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)
63868-024-15
11-Digit CMS (5-4-2)
63868-0024-15

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