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  5. NDC Package Code: 50436-1570-1 Bupropion Hydrochloride

NDC Package 50436-1570-1 Bupropion Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

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 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:
50436-1570-1
Package Description:
30 TABLET, FILM COATED in 1 BOTTLE
Product Code:
50436-1570
Proprietary Name:
Bupropion Hydrochloride
Usage Information:
Bupropion hydrochloride tablets are indicated for the treatment of major depressive disorder (MDD), as defined by the Diagnostic and Statistical Manual (DSM). The efficacy of bupropion hydrochloride tablets 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)].
11-Digit NDC Billing Format:
50436157001
NDC to RxNorm Crosswalk:
  • RxCUI: 993687 - buPROPion HCl 100 MG Oral Tablet
  • RxCUI: 993687 - bupropion hydrochloride 100 MG Oral Tablet
  • RxCUI: 993691 - buPROPion HCl 75 MG Oral Tablet
  • RxCUI: 993691 - bupropion hydrochloride 75 MG Oral Tablet
  • RxCUI: 993691 - bupropion HCl 75 MG Oral Tablet
    • Labeler Name:
    Unit Dose Services
    Sample Package:
    No
    Start Marketing Date:
    01-17-2006
    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.

    Frequently Asked Questions

    What is NDC 50436-1570-1?

    The NDC Packaged Code 50436-1570-1 is assigned to a package of 30 tablet, film coated in 1 bottle of Bupropion Hydrochloride, labeled by Unit Dose Services. The product's dosage form is and is administered via form.

    Is NDC 50436-1570 included in the NDC Directory?

    No, Bupropion Hydrochloride with product code 50436-1570 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 January 17, 2006 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 50436-1570-1?

    The 11-digit format is 50436157001. 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
    5-4-150436-1570-15-4-250436-1570-01