NDC Package 68382-032-01 Divalproex Sodium

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:

68382-032-01

Package Description:

100 TABLET, DELAYED RELEASE in 1 BOTTLE

Product Code:

68382-032

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:

68382003201

Billing Unit:

EA - Billing unit of "each" is used when the product is dispensed in discreet units.

NDC to RxNorm Crosswalk:

100 EA

Labeler Name:

Zydus Pharmaceuticals Usa Inc.

Sample Package:

FDA Application Number:

ANDA077100

Marketing Category:

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

Start Marketing Date:

03-06-2010

End Marketing Date:

04-02-2025

Listing Expiration Date:

04-02-2025

Exclude Flag:

Code Structure:

68382 - Zydus Pharmaceuticals Usa Inc.
- 68382-032 - Divalproex Sodium
  - 68382-032-01 - 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
68382-032-05	500 TABLET, DELAYED RELEASE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 68382-032-01?

The NDC Packaged Code 68382-032-01 is assigned to a package of 100 tablet, delayed release in 1 bottle of Divalproex Sodium, labeled by Zydus Pharmaceuticals Usa Inc.. The product's dosage form is and is administered via form.

Is NDC 68382-032 included in the NDC Directory?

No, Divalproex Sodium with product code 68382-032 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Zydus Pharmaceuticals Usa Inc. on March 06, 2010 and its listing in the NDC Directory is set to expire on April 02, 2025 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 68382-032-01?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 100.

What is the 11-digit format for NDC 68382-032-01?

The 11-digit format is 68382003201. 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	68382-032-01	5-4-2	68382-0032-01

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