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  5. NDC Package Code: 50742-611-01 Oxcarbazepine

NDC Package 50742-611-01 Oxcarbazepine

Tablet, Extended Release 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:
50742-611-01
Package Description:
100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Code:
50742-611
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:
50742061101
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
100 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1365653 - OXcarbazepine 150 MG 24HR Extended Release Oral Tablet
  • RxCUI: 1365653 - 24 HR oxcarbazepine 150 MG Extended Release Oral Tablet
  • RxCUI: 1365653 - oxcarbazepine 150 MG 24 HR Extended Release Oral Tablet
  • RxCUI: 1365842 - OXcarbazepine 300 MG 24HR Extended Release Oral Tablet
  • RxCUI: 1365842 - 24 HR oxcarbazepine 300 MG Extended Release Oral Tablet
Product Type:
Human Prescription Drug
Labeler Name:
Ingenus Pharmaceuticals, Llc
Dosage Form:
Tablet, Extended Release - A solid dosage form containing a drug which allows at least a reduction in dosing frequency as compared to that drug presented in conventional dosage form.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
OXCARBAZEPINE 150 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA215796
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
06-01-2025
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 50742-611-01?

The NDC Packaged Code 50742-611-01 is assigned to a package of 100 tablet, extended release in 1 bottle, plastic of Oxcarbazepine, a human prescription drug labeled by Ingenus Pharmaceuticals, Llc. The product's dosage form is tablet, extended release and is administered via oral form.

Is NDC 50742-611 included in the NDC Directory?

Yes, Oxcarbazepine with product code 50742-611 is active and included in the NDC Directory. The product was first marketed by Ingenus Pharmaceuticals, Llc on June 01, 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 NDC billing unit for package 50742-611-01?

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 50742-611-01?

The 11-digit format is 50742061101. 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
5-3-250742-611-015-4-250742-0611-01