Donepezil Hydrochloride

Product NDC

0781-5275

11-digit product format

007815275

Labeler code

0781

Product ID

0781-5275_a878e36d-bdf5-43ff-8f8a-b5a1d16f1e30

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Donepezil Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Sandoz Inc

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