Donepezil Hydrochloride

Product NDC

52343-090

11-digit product format

523430090

Labeler code

52343

Product ID

52343-090_4df75984-d56d-41f2-8bb9-9a9b241194f0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Donepezil Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

ACETRIS HEALTH, LLC

Application

ANDA090056

Marketing category

ANDA

Marketing start

2011-05-31

Marketing end

2020-01-01

Substance

DONEPEZIL HYDROCHLORIDE

Active strength

10 mg/1

Pharmacologic classes

Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record