NDC Package 62856-246-41 Aricept

Donepezil Hydrochloride Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

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:
62856-246-41
Package Description:
10 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Aricept
Non-Proprietary Name:
Donepezil Hydrochloride
Substance Name:
Donepezil Hydrochloride
Usage Information:
Donepezil is used to treat confusion (dementia) related to Alzheimer's disease. It does not cure Alzheimer's disease, but it may improve memory, awareness, and the ability to function. This medication is an enzyme blocker that works by restoring the balance of natural substances (neurotransmitters) in the brain.
11-Digit NDC Billing Format:
62856024641
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
10 EA
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Eisai Inc.
Dosage Form:
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Sample Package:
No
FDA Application Number:
NDA020690
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
11-25-1996
Listing Expiration Date:
12-31-2025
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
62856-246-111000 TABLET, FILM COATED in 1 BOTTLE
62856-246-3030 TABLET, FILM COATED in 1 BOTTLE
62856-246-9090 TABLET, FILM COATED in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 62856-246-41?

The NDC Packaged Code 62856-246-41 is assigned to a package of 10 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack of Aricept, a human prescription drug labeled by Eisai Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

Is NDC 62856-246 included in the NDC Directory?

Yes, Aricept with product code 62856-246 is active and included in the NDC Directory. The product was first marketed by Eisai Inc. on November 25, 1996 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 62856-246-41?

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 10.

What is the 11-digit format for NDC 62856-246-41?

The 11-digit format is 62856024641. 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
5-3-262856-246-415-4-262856-0246-41