NDC Package 65862-401-10 Divalproex Sodium

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:

65862-401-10

Package Description:

10 BLISTER PACK in 1 CARTON / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK

Product Code:

65862-401

Proprietary Name:

Divalproex Sodium

Usage Information:

This medication is used to treat seizure disorders, certain psychiatric conditions (manic phase of bipolar disorder), and to prevent migraine headaches. It works by restoring the balance of certain natural substances (neurotransmitters) in the brain.

11-Digit NDC Billing Format:

65862040110

Labeler Name:

Aurobindo Pharma Limited

Sample Package:

FDA Application Number:

ANDA090554

Marketing Category:

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

Start Marketing Date:

04-21-2011

End Marketing Date:

10-30-2015

Listing Expiration Date:

10-30-2015

Exclude Flag:

Code Structure:

65862 - Aurobindo Pharma Limited
- 65862-401 - Divalproex Sodium
  - 65862-401-10 - 10 BLISTER PACK in 1 CARTON / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK

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
65862-401-01	100 TABLET, DELAYED RELEASE in 1 BOTTLE
65862-401-05	500 TABLET, DELAYED RELEASE in 1 BOTTLE
65862-401-71	7000 TABLET, DELAYED RELEASE in 1 BOTTLE
65862-401-99	1000 TABLET, DELAYED RELEASE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 65862-401-10?

The NDC Packaged Code 65862-401-10 is assigned to a package of 10 blister pack in 1 carton / 10 tablet, delayed release in 1 blister pack of Divalproex Sodium, labeled by Aurobindo Pharma Limited. The product's dosage form is and is administered via form.

Is NDC 65862-401 included in the NDC Directory?

No, Divalproex Sodium with product code 65862-401 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Aurobindo Pharma Limited on April 21, 2011 and its listing in the NDC Directory is set to expire on October 30, 2015 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 65862-401-10?

The 11-digit format is 65862040110. 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	65862-401-10	5-4-2	65862-0401-10

Table of Contents