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  5. NDC Package Code: 67046-699-30 Bupropion XL

NDC Package 67046-699-30 Bupropion XL

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:
67046-699-30
Package Description:
30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product Code:
67046-699
Proprietary Name:
Bupropion XL
Usage Information:
This medication is used to treat depression. It may also be used to prevent seasonal affective disorder (SAD), a type of depression that occurs each year at the same time (for example, during winter). This medication can improve your mood and feelings of well-being. It may work by restoring the balance of certain natural substances (dopamine, norepinephrine) in the brain.
11-Digit NDC Billing Format:
67046069930
NDC to RxNorm Crosswalk:
  • RxCUI: 993541 - buPROPion HCl 150 MG 24HR Extended Release Oral Tablet
  • RxCUI: 993541 - 24 HR bupropion hydrochloride 150 MG Extended Release Oral Tablet
  • RxCUI: 993541 - bupropion HCl XL 150 MG 24 HR Extended Release Oral Tablet
Labeler Name:
Coupler Enterprises Inc
Sample Package:
No
FDA Application Number:
ANDA090693
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
02-14-2017
Listing Expiration Date:
12-31-2021
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 67046-699-30?

The NDC Packaged Code 67046-699-30 is assigned to a package of 30 tablet, extended release in 1 blister pack of Bupropion XL, labeled by Coupler Enterprises Inc. The product's dosage form is and is administered via form.

Is NDC 67046-699 included in the NDC Directory?

No, Bupropion XL with product code 67046-699 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Coupler Enterprises Inc on February 14, 2017 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 67046-699-30?

The 11-digit format is 67046069930. 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 5-3-2 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
5-3-267046-699-305-4-267046-0699-30