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  5. NDC Package Code: 72322-1043-2 Divalproex Sodium

NDC Package 72322-1043-2 Divalproex Sodium

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory .

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:
72322-1043-2
Package Description:
500 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Code:
72322-1043
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:
72322104302
Labeler Name:
Amta Labs Limited
Sample Package:
No
FDA Application Number:
ANDA214462
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
11-10-2021
End Marketing Date:
11-10-2021
Listing Expiration Date:
11-10-2021
Exclude Flag:
D
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
72322-1043-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 72322-1043-2?

The NDC Packaged Code 72322-1043-2 is assigned to a package of 500 tablet, extended release in 1 bottle of Divalproex Sodium, labeled by Amta Labs Limited. The product's dosage form is and is administered via form.

Is NDC 72322-1043 included in the NDC Directory?

The product was first marketed by Amta Labs Limited on November 10, 2021 and its listing in the NDC Directory is set to expire on November 10, 2021 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 72322-1043-2?

The 11-digit format is 72322104302. 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 5-4-1 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
5-4-172322-1043-25-4-272322-1043-02