NDC Package 71335-1551-4 Bupropion Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Package Information
Other Packages
Frequently Asked Questions

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:

71335-1551-4

Package Description:

7 TABLET, FILM COATED in 1 BOTTLE

Product Code:

71335-1551

Proprietary Name:

Bupropion Hydrochloride

Usage Information:

Bupropion hydrochloride tablets USP 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 USP 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:

71335155104

NDC to RxNorm Crosswalk:

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:

Bryant Ranch Prepack

Sample Package:

FDA Application Number:

ANDA203013

Marketing Category:

ANDA - A product marketed under an approved Abbreviated New Drug Application.

Start Marketing Date:

06-18-2018

End Marketing Date:

01-15-2024

Listing Expiration Date:

01-15-2024

Exclude Flag:

Code Structure:

71335 - Bryant Ranch Prepack
- 71335-1551 - Bupropion Hydrochloride
  - 71335-1551-4 - 7 TABLET, FILM COATED in 1 BOTTLE

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 Code	Package Description
71335-1551-1	30 TABLET, FILM COATED in 1 BOTTLE
71335-1551-2	60 TABLET, FILM COATED in 1 BOTTLE
71335-1551-3	90 TABLET, FILM COATED in 1 BOTTLE
71335-1551-5	14 TABLET, FILM COATED in 1 BOTTLE
71335-1551-6	120 TABLET, FILM COATED in 1 BOTTLE
71335-1551-7	100 TABLET, FILM COATED in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 71335-1551-4?

The NDC Packaged Code 71335-1551-4 is assigned to a package of 7 tablet, film coated in 1 bottle of Bupropion Hydrochloride, labeled by Bryant Ranch Prepack. The product's dosage form is and is administered via form.

Is NDC 71335-1551 included in the NDC Directory?

No, Bupropion Hydrochloride with product code 71335-1551 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Bryant Ranch Prepack on June 18, 2018 and its listing in the NDC Directory is set to expire on January 15, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 71335-1551-4?

The 11-digit format is 71335155104. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-4-1	71335-1551-4	5-4-2	71335-1551-04

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