Felodipine
NDC Package 54738-080-03

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.

Felodipine is a . Marketed by Richmond Pharmaceuticals, Inc., this product is identified by NDC 54738-080 and is authorized under FDA application ANDA075896.

Identification & Billing

NDC Package Code
54738-080-03
Package Description
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Code
54738-080
11-Digit Billing Format
54738008003

Clinical Specifications

Proprietary Name
Felodipine
Dosage Form
-

Regulatory & Marketing

Labeler Name
Richmond Pharmaceuticals, Inc.
FDA Application #
ANDA075896
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
07-23-2012
End Marketing Date
07-24-2012
Listing Expiration
07-24-2012
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 (54738-080). Click a package code to view its specific billing and regulatory data.

54738-080-90
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

* 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 54738-080-03 identifies a specific commercial package of 1000 tablet, film coated, extended release in 1 bottle, plastic of Felodipine, labeled by Richmond 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 Richmond Pharmaceuticals, Inc. on July 23, 2012. The current certification is valid through July 24, 2012.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 54738008003. 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)
54738-080-03
11-Digit CMS (5-4-2)
54738-0080-03

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