NDC Package 62856-584-46 Banzel

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

Package Information
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:

62856-584-46

Package Description:

1 BOTTLE in 1 CARTON / 460 mL in 1 BOTTLE

Product Code:

62856-584

Proprietary Name:

Banzel

Non-Proprietary Name:

Rufinamide

Substance Name:

Rufinamide

Usage Information:

Rufinamide is used with other medications to prevent or control seizures (epilepsy) associated with Lennox-Gastaut syndrome (LGS). This medication is an anticonvulsant. Rufinamide is thought to work by acting on the sodium channels in the brain that carry excessive electrical charges that may cause seizures.

11-Digit NDC Billing Format:

62856058446

Billing Unit:

ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.

NDC to RxNorm Crosswalk:

RxCUI: 1092357 - rufinamide 40 MG in 1 mL Oral Suspension

RxCUI: 1092357 - rufinamide 40 MG/ML Oral Suspension

RxCUI: 1092357 - rufinamide 40 MG per 1 ML Oral Suspension

RxCUI: 1092360 - BANZEL 40 MG in 1 mL Oral Suspension

RxCUI: 1092360 - rufinamide 40 MG/ML Oral Suspension [Banzel]

Product Type:

Human Prescription Drug

Labeler Name:

Eisai 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):

RUFINAMIDE 40 mg/mL

Sample Package:

FDA Application Number:

NDA201367

Marketing Category:

NDA - A product marketed under an approved New Drug Application.

Start Marketing Date:

03-03-2011

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

62856 - Eisai Inc.
- 62856-584 - Banzel
  - 62856-584-46 - 1 BOTTLE in 1 CARTON / 460 mL in 1 BOTTLE

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 62856-584-46?

The NDC Packaged Code 62856-584-46 is assigned to a package of 1 bottle in 1 carton / 460 ml in 1 bottle of Banzel, a human prescription drug labeled by Eisai Inc.. The product's dosage form is suspension and is administered via oral form.

Is NDC 62856-584 included in the NDC Directory?

Yes, Banzel with product code 62856-584 is active and included in the NDC Directory. The product was first marketed by Eisai Inc. on March 03, 2011 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 62856-584-46?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

What is the 11-digit format for NDC 62856-584-46?

The 11-digit format is 62856058446. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	62856-584-46	5-4-2	62856-0584-46

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