Donepezil Hydrochloride

Product NDC

0904-6408

11-digit product format

009046408

Labeler code

0904

Product ID

0904-6408_86a17f3c-5e3d-42ed-8d8c-dc07e5ee2695

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Donepezil Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Major Pharmaceuticals

Application

ANDA201724

Marketing category

ANDA

Marketing start

2016-01-29

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