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  5. NDC Package Code: 62332-821-71 Divalproex Sodium

NDC Package 62332-821-71 Divalproex Sodium

Capsule, Delayed Release Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

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

Package Information

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:
62332-821-71
Package Description:
500 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product Code:
62332-821
Proprietary Name:
Divalproex Sodium
Non-Proprietary Name:
Divalproex Sodium
Substance 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:
62332082171
NDC to RxNorm Crosswalk:
RxCUI: 1099596 - divalproex sodium 125 MG Delayed Release Oral Capsule
Product Type:
Human Prescription Drug
Labeler Name:
Alembic Pharmaceuticals Inc.
Dosage Form:
Capsule, Delayed Release - A solid dosage form in which the drug is enclosed within either a hard or soft soluble container made from a suitable form of gelatin, and which releases a drug (or drugs) at a time other than promptly after administration. Enteric-coated articles are delayed release dosage forms.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
DIVALPROEX SODIUM 125 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA218793
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
12-23-2024
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
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
62332-821-10100 BLISTER PACK in 1 CARTON / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
62332-821-31100 CAPSULE, DELAYED RELEASE in 1 BOTTLE
62332-821-911000 CAPSULE, DELAYED RELEASE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 62332-821-71?

The NDC Packaged Code 62332-821-71 is assigned to a package of 500 capsule, delayed release in 1 bottle of Divalproex Sodium, a human prescription drug labeled by Alembic Pharmaceuticals Inc.. The product's dosage form is capsule, delayed release and is administered via oral form.

Is NDC 62332-821 included in the NDC Directory?

Yes, Divalproex Sodium with product code 62332-821 is active and included in the NDC Directory. The product was first marketed by Alembic Pharmaceuticals Inc. on December 23, 2024 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 62332-821-71?

The 11-digit format is 62332082171. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-262332-821-715-4-262332-0821-71