NDC Package 24979-514-10 Divalproex Sodium Delayed-release

View Billable Units, 11-Digit Format, RxNorm

Package Information
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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:

24979-514-10

Package Description:

100 TABLET, DELAYED RELEASE in 1 BOTTLE

Product Code:

24979-514

Proprietary Name:

Divalproex Sodium Delayed-release

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:

24979051410

Labeler Name:

Twi Pharmaceuticals, Inc.

Sample Package:

FDA Application Number:

ANDA078411

Marketing Category:

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

Start Marketing Date:

06-01-2011

End Marketing Date:

09-20-2013

Listing Expiration Date:

09-20-2013

Exclude Flag:

Code Structure:

24979 - Twi Pharmaceuticals, Inc.
- 24979-514 - Divalproex Sodium
  - 24979-514-10 - 100 TABLET, DELAYED 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
24979-514-50	500 TABLET, DELAYED RELEASE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 24979-514-10?

The NDC Packaged Code 24979-514-10 is assigned to a package of 100 tablet, delayed release in 1 bottle of Divalproex Sodium Delayed-release, labeled by Twi Pharmaceuticals, Inc.. The product's dosage form is and is administered via form.

Is NDC 24979-514 included in the NDC Directory?

No, Divalproex Sodium Delayed-release with product code 24979-514 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Twi Pharmaceuticals, Inc. on June 01, 2011 and its listing in the NDC Directory is set to expire on September 20, 2013 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 24979-514-10?

The 11-digit format is 24979051410. 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	24979-514-10	5-4-2	24979-0514-10

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