Donepezil

Product NDC

68071-3192

11-digit product format

680713192

Labeler code

68071

Product ID

68071-3192_521b206c-e736-4a82-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Donepezil hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA203034

Marketing category

ANDA

Marketing start

2015-02-02

Marketing end

0000-00-00

Substance

DONEPEZIL HYDROCHLORIDE

Active strength

5 mg/1

Pharmacologic classes

Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record