Donepezil Hydrochloride

Product NDC

60687-171

11-digit product format

606870171

Labeler code

60687

Product ID

60687-171_5918103a-5bb2-45b8-e053-2991aa0a246f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Donepezil Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

American Health Packaging

Application

ANDA201146

Marketing category

ANDA

Marketing start

2015-07-15

Marketing end

2019-03-31

Substance

DONEPEZIL HYDRO

Active strength

5 mg/1

Pharmacologic classes

Cholinesterase

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record