Bupropion Hydrochloride
NDC Package 72189-252-90

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.

Bupropion Hydrochloride is a . Marketed by Direct Rx, this product is identified by NDC 72189-252 and is authorized under FDA application ANDA210497.

Identification & Billing

NDC Package Code
72189-252-90
Package Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Code
72189-252
11-Digit Billing Format
72189025290
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
90 EA

Clinical Specifications

Proprietary Name
Bupropion Hydrochloride
Dosage Form
-

Regulatory & Marketing

Labeler Name
Direct Rx
FDA Application #
ANDA210497
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
11-15-2021
End Marketing Date
12-17-2021
Listing Expiration
12-17-2021
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 72189-252-90 identifies a specific commercial package of 90 tablet, extended release in 1 bottle of Bupropion Hydrochloride, labeled by Direct Rx. This product is billed for "EA" each discreet unit and contains an estimated amount of 90 billable units per package. 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 Direct Rx on November 15, 2021. The current certification is valid through December 17, 2021.

How is this Direct Rx product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72189025290. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 90 total billable units per package. 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)
72189-252-90
11-Digit CMS (5-4-2)
72189-0252-90

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