NDC Package 84054-005-60 Zunveyl

Benzgalantamine Tablet, Delayed Release 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:
84054-005-60
Package Description:
60 TABLET, DELAYED RELEASE in 1 BOTTLE
Product Code:
Proprietary Name:
Zunveyl
Non-Proprietary Name:
Benzgalantamine
Substance Name:
Benzgalantamine
Usage Information:
ZUNVEYL is indicated for the treatment of mild to moderate dementia of the Alzheimer's type in adults.
11-Digit NDC Billing Format:
84054000560
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
60 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 2690632 - benzgalantamine 5 MG Delayed Release Oral Tablet
  • RxCUI: 2690632 - benzgalantamine 5 MG (equivalent to benzgalantamine gluconate 7.49 MG) Delayed Release Oral Tablet
  • RxCUI: 2690638 - ZUNVEYL 5 MG Delayed Release Oral Tablet
  • RxCUI: 2690638 - benzgalantamine 5 MG Delayed Release Oral Tablet [Zunveyl]
  • RxCUI: 2690638 - Zunveyl 5 MG Delayed Release Oral Tablet
Product Type:
Human Prescription Drug
Labeler Name:
Alpha Cognition, Inc.
Dosage Form:
Tablet, Delayed Release - A solid dosage form which releases a drug (or drugs) at a time other than promptly after administration. Enteric-coated articles are delayed release dosage forms.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Sample Package:
No
FDA Application Number:
NDA218549
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
08-09-2024
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.

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Frequently Asked Questions

What is NDC 84054-005-60?

The NDC Packaged Code 84054-005-60 is assigned to a package of 60 tablet, delayed release in 1 bottle of Zunveyl, a human prescription drug labeled by Alpha Cognition, Inc.. The product's dosage form is tablet, delayed release and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 60 billable units per package.

Is NDC 84054-005 included in the NDC Directory?

Yes, Zunveyl with product code 84054-005 is active and included in the NDC Directory. The product was first marketed by Alpha Cognition, Inc. on August 09, 2024 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 84054-005-60?

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 60.

What is the 11-digit format for NDC 84054-005-60?

The 11-digit format is 84054000560. 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
5-3-284054-005-605-4-284054-0005-60