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  5. NDC Package Code: 50436-0289-1 Bupropion

NDC Package 50436-0289-1 Bupropion

View Billable Units, 11-Digit Format, RxNorm

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 inactivated by the FDA.

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:
50436-0289-1
Package Description:
57 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Code:
50436-0289
Proprietary Name:
Bupropion
Usage Information:
Bupropion Hydrochloride Extended-release (SR) tablets 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 [see Clinical Studies (14)].The efficacy of Bupropion Hydrochloride Extended-release (SR) tablets in maintaining an antidepressant response for up to 44 weeks following 8 weeks of acute treatment was demonstrated in a placebo-controlled trial [see Clinical Studies (14)].
11-Digit NDC Billing Format:
50436028901
NDC to RxNorm Crosswalk:
  • RxCUI: 993518 - buPROPion HCl 150 MG 12HR Extended Release Oral Tablet
  • RxCUI: 993518 - 12 HR bupropion hydrochloride 150 MG Extended Release Oral Tablet
  • RxCUI: 993518 - bupropion HCl 150 MG 12 HR Extended Release Oral Tablet
    • Labeler Name:
    Unit Dose Services
    Sample Package:
    No
    Start Marketing Date:
    11-01-2014
    Listing Expiration Date:
    12-31-2020
    Exclude Flag:
    I
    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
    50436-0289-260 TABLET, EXTENDED RELEASE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50436-0289-1?

    The NDC Packaged Code 50436-0289-1 is assigned to a package of 57 tablet, extended release in 1 bottle of Bupropion, labeled by Unit Dose Services. The product's dosage form is and is administered via form.

    Is NDC 50436-0289 included in the NDC Directory?

    No, Bupropion with product code 50436-0289 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Unit Dose Services on November 01, 2014 and its listing in the NDC Directory is set to expire on December 31, 2020 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 50436-0289-1?

    The 11-digit format is 50436028901. 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 5-4-1 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
    5-4-150436-0289-15-4-250436-0289-01