NDC Package 0185-0415-60 Bupropion Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Package Information

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

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
0185-0415-60
Package Description:
60 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Code:
Proprietary Name:
Bupropion Hydrochloride
Usage Information:
Bupropion hydrochloride extended-release tablets (SR) are indicated for the treatment of major depressive disorder (MDD), as defined by the Diagnostic and Statistical Manual (DSM). The efficacy of bupropion in the treatment of a major depressive episode was established in two 4-week controlled inpatient trials and one 6-week controlled outpatient trial of adult subjects with MDD [seeClinical Studies (14)].The efficacy of bupropion hydrochloride extended-release tablets (SR) in maintaining an antidepressant response for up to 44 weeks following 8 weeks of acute treatment was demonstrated in a placebo-controlled trial [seeClinical Studies (14)].
11-Digit NDC Billing Format:
00185041560
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
60 EA
Labeler Name:
Eon Labs, Inc.
Sample Package:
No
FDA Application Number:
ANDA075932
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
03-22-2004
End Marketing Date:
07-31-2025
Listing Expiration Date:
07-31-2025
Exclude Flag:
D
Code Structure:

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 disclaimer below.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
0185-0415-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE
0185-0415-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE
0185-0415-52250 TABLET, EXTENDED RELEASE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 0185-0415-60?

The NDC Packaged Code 0185-0415-60 is assigned to a package of 60 tablet, extended release in 1 bottle of Bupropion Hydrochloride, labeled by Eon Labs, Inc.. The product's dosage form is and is administered via form.

Is NDC 0185-0415 included in the NDC Directory?

No, Bupropion Hydrochloride with product code 0185-0415 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Eon Labs, Inc. on March 22, 2004 and its listing in the NDC Directory is set to expire on July 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 0185-0415-60?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 60.

What is the 11-digit format for NDC 0185-0415-60?

The 11-digit format is 00185041560. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 4-4-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
4-4-20185-0415-605-4-200185-0415-60