NDC Package 41616-760-18 Venlafaxine 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:

41616-760-18

Package Description:

1000 TABLET, EXTENDED RELEASE in 1 BOTTLE

Product Code:

41616-760

Proprietary Name:

Venlafaxine Hydrochloride

11-Digit NDC Billing Format:

41616076018

Labeler Name:

Sun Pharma Global Inc.

Sample Package:

FDA Application Number:

ANDA091272

Marketing Category:

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

Start Marketing Date:

08-18-2010

End Marketing Date:

03-31-2016

Listing Expiration Date:

03-31-2016

Exclude Flag:

Code Structure:

41616 - Sun Pharma Global Inc.
- 41616-760 - Venlafaxine Hydrochloride
  - 41616-760-18 - 1000 TABLET, EXTENDED RELEASE 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
41616-760-08	100 TABLET, EXTENDED RELEASE in 1 BOTTLE
41616-760-81	90 TABLET, EXTENDED RELEASE in 1 BOTTLE
41616-760-83	30 TABLET, EXTENDED RELEASE in 1 BOTTLE
41616-760-88	100 TABLET, EXTENDED RELEASE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 41616-760-18?

The NDC Packaged Code 41616-760-18 is assigned to a package of 1000 tablet, extended release in 1 bottle of Venlafaxine Hydrochloride, labeled by Sun Pharma Global Inc.. The product's dosage form is and is administered via form.

Is NDC 41616-760 included in the NDC Directory?

No, Venlafaxine Hydrochloride with product code 41616-760 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Sun Pharma Global Inc. on August 18, 2010 and its listing in the NDC Directory is set to expire on March 31, 2016 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 41616-760-18?

The 11-digit format is 41616076018. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	41616-760-18	5-4-2	41616-0760-18

Table of Contents