Donepezil hydrochloride

Product NDC

0615-7654

11-digit product format

006157654

Labeler code

0615

Product ID

0615-7654_7879f700-695d-4ab5-b3b3-dfbb349853a7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Donepezil hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA201001

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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record