Granisetron Hydrochloride
NDC Package 43975-226-80

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.

Granisetron Hydrochloride is a . Marketed by Amerigen Pharmaceuticals, Inc, this product is identified by NDC 43975-226 and is authorized under FDA application ANDA078969.

Identification & Billing

NDC Package Code
43975-226-80
Package Description
2 BLISTER PACK in 1 PACKAGE / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product Code
43975-226
11-Digit Billing Format
43975022680

Clinical Specifications

Proprietary Name
Granisetron Hydrochloride
Dosage Form
-

Regulatory & Marketing

Labeler Name
Amerigen Pharmaceuticals, Inc
FDA Application #
ANDA078969
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
03-16-1995
End Marketing Date
05-10-2010
Listing Expiration
05-10-2010
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 (43975-226). Click a package code to view its specific billing and regulatory data.

43975-226-81
1 BLISTER PACK in 1 PACKAGE / 2 TABLET, FILM COATED 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 43975-226-80 identifies a specific commercial package of 2 blister pack in 1 package / 10 tablet, film coated in 1 blister pack of Granisetron Hydrochloride, labeled by Amerigen Pharmaceuticals, Inc. 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 Amerigen Pharmaceuticals, Inc on March 16, 1995. The current certification is valid through May 10, 2010.

How is this Amerigen Pharmaceuticals, Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43975022680. 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)
43975-226-80
11-Digit CMS (5-4-2)
43975-0226-80

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