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  5. NDC Package Code: 51672-1393-1 Oxcarbazepine

NDC Package 51672-1393-1 Oxcarbazepine

Suspension Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
51672-1393-1
Package Description:
1 BOTTLE, GLASS in 1 CARTON / 250 mL in 1 BOTTLE, GLASS
Product Code:
51672-1393
Proprietary Name:
Oxcarbazepine
Non-Proprietary Name:
Oxcarbazepine
Substance Name:
Oxcarbazepine
Usage Information:
Oxcarbazepine is used alone or with other medications to treat seizure disorders (epilepsy).
11-Digit NDC Billing Format:
51672139301
Product Type:
Human Prescription Drug
Labeler Name:
Sun Pharmaceutical Industries, Inc.
Dosage Form:
Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
OXCARBAZEPINE 60 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA078734
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
08-06-2025
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.

Frequently Asked Questions

What is NDC 51672-1393-1?

The NDC Packaged Code 51672-1393-1 is assigned to a package of 1 bottle, glass in 1 carton / 250 ml in 1 bottle, glass of Oxcarbazepine, a human prescription drug labeled by Sun Pharmaceutical Industries, Inc.. The product's dosage form is suspension and is administered via oral form.

Is NDC 51672-1393 included in the NDC Directory?

Yes, Oxcarbazepine with product code 51672-1393 is active and included in the NDC Directory. The product was first marketed by Sun Pharmaceutical Industries, Inc. on August 06, 2025 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 51672-1393-1?

The 11-digit format is 51672139301. 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
5-4-151672-1393-15-4-251672-1393-01