Donepezil Hydrochloride

Product NDC

63739-678

11-digit product format

637390678

Labeler code

63739

Product ID

63739-678_b716e395-5442-40a1-9345-e2fe00a73c71

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Donepezil Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

McKesson Corporation dba SKY Packaging

Application

ANDA090290

Marketing category

ANDA

Marketing start

2011-05-31

Marketing end

0000-00-00

Substance

DONEPEZIL HYDROCHLORIDE

Active strength

10 mg/1

Pharmacologic classes

Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record