Proamatine
NDC Package 54092-003-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Proamatine is a . Marketed by Takeda Pharmaceuticals America, Inc., this product is identified by NDC 54092-003 and is authorized under FDA application NDA019815.

Identification & Billing

NDC Package Code
54092-003-01
Package Description
100 TABLET in 1 BOTTLE
Product Code
54092-003
11-Digit Billing Format
54092000301

Clinical Specifications

Proprietary Name
Proamatine
Dosage Form
-

Regulatory & Marketing

Labeler Name
Takeda Pharmaceuticals America, Inc.
FDA Application #
NDA019815
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
09-06-1996
End Marketing Date
12-31-2010
Listing Expiration
12-31-2010
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 54092-003-01 identifies a specific commercial package of 100 tablet in 1 bottle of Proamatine, labeled by Takeda Pharmaceuticals America, 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 Takeda Pharmaceuticals America, Inc. on September 06, 1996. The current certification is valid through December 31, 2010.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 54092000301. 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)
54092-003-01
11-Digit CMS (5-4-2)
54092-0003-01

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