NDC Package 69680-183-30 Memantine Hydrochloride And Donepezil Hydrochloride

Capsule, Extended 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:
69680-183-30
Package Description:
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Product Code:
Proprietary Name:
Memantine Hydrochloride And Donepezil Hydrochloride
Non-Proprietary Name:
Memantine Hydrochloride And Donepezil Hydrochloride
Substance Name:
Donepezil Hydrochloride; Memantine Hydrochloride
Usage Information:
Memantine and donepezil hydrochlorides extended-release capsulesĀ is indicated for the treatment of moderate to severe dementia of the Alzheimer's type in patients stabilized on 10 mg of donepezil hydrochloride once daily.
11-Digit NDC Billing Format:
69680018330
NDC to RxNorm Crosswalk:
  • RxCUI: 1599803 - donepezil HCl 10 MG / memantine HCl 28 MG 24HR Extended Release Oral Capsule
  • RxCUI: 1599803 - 24 HR donepezil hydrochloride 10 MG / memantine hydrochloride 28 MG Extended Release Oral Capsule
  • RxCUI: 1599803 - donepezil hydrochloride 10 MG / memantine hydrochloride 28 MG 24 HR Extended Release Oral Capsule
  • RxCUI: 1599805 - donepezil HCl 10 MG / memantine HCl 14 MG 24HR Extended Release Oral Capsule
  • RxCUI: 1599805 - 24 HR donepezil hydrochloride 10 MG / memantine hydrochloride 14 MG Extended Release Oral Capsule
Product Type:
Human Prescription Drug
Labeler Name:
Vitruvias Therapeutics, Inc.
Dosage Form:
Capsule, Extended Release - A solid dosage form in which the drug is enclosed within either a hard or soft soluble container made from a suitable form of gelatin, and which releases a drug (or drugs) in such a manner to allow a reduction in dosing frequency as compared to that drug (or drugs) presented as a conventional dosage form.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Sample Package:
No
FDA Application Number:
ANDA216901
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
07-16-2025
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.

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Frequently Asked Questions

What is NDC 69680-183-30?

The NDC Packaged Code 69680-183-30 is assigned to a package of 30 capsule, extended release in 1 bottle of Memantine Hydrochloride And Donepezil Hydrochloride, a human prescription drug labeled by Vitruvias Therapeutics, Inc.. The product's dosage form is capsule, extended release and is administered via oral form.

Is NDC 69680-183 included in the NDC Directory?

Yes, Memantine Hydrochloride And Donepezil Hydrochloride with product code 69680-183 is active and included in the NDC Directory. The product was first marketed by Vitruvias Therapeutics, Inc. on July 16, 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 11-digit format for NDC 69680-183-30?

The 11-digit format is 69680018330. 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
5-3-269680-183-305-4-269680-0183-30