Oxcarbazepine For Suspension
NDC Package 33342-259-67

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Oxcarbazepine for suspensions is oxcarbazepine is used alone or with other medications to treat seizure disorders (epilepsy). This formulation utilizes a for suspension delivery system. Marketed by Macleods Pharmaceuticals Limited, this product is identified by NDC 33342-259 and is authorized under FDA application ANDA207300.

Identification & Billing

NDC Package Code
33342-259-67
Package Description
1 BOTTLE in 1 CARTON / 250 mL in 1 BOTTLE
Product Code
11-Digit Billing Format
33342025967
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Oxcarbazepine
Non-Proprietary Name
Oxcarbazepine
Substance Name
Oxcarbazepine
Dosage Form
For Suspension - A product, usually a solid, intended for suspension prior to administration.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
Oxcarbazepine is used alone or with other medications to treat seizure disorders (epilepsy).

Regulatory & Marketing

Labeler Name
Macleods Pharmaceuticals Limited
Product Type
Human Prescription Drug
FDA Application #
ANDA207300
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
07-11-2025
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 33342-259-67 identifies a specific commercial package of 1 bottle in 1 carton / 250 ml in 1 bottle of Oxcarbazepine, a human prescription drug labeled by Macleods Pharmaceuticals Limited. This for suspension is formulated for oral use and contains oxcarbazepine as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Macleods Pharmaceuticals Limited on July 11, 2025. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

Oxcarbazepine is used alone or with other medications to treat seizure disorders (epilepsy).

How is this Macleods Pharmaceuticals Limited product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 33342025967. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
33342-259-67
11-Digit CMS (5-4-2)
33342-0259-67

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.