Donepezil hydrochloride

Product NDC

49884-232

11-digit product format

498840232

Labeler code

49884

Product ID

49884-232_9081d379-7a9d-4501-a22c-7448155efd24

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Donepezil hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Par Pharmaceutical, Inc.

Application

ANDA202542

Marketing category

ANDA

Marketing start

2013-09-15

Marketing end

2020-07-31

Substance

DONEPEZIL HYDROCHLORIDE

Active strength

23 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