Donepezil Hydrochloride

Product NDC
0781-5274
11-digit product format
007815274
Labeler code
0781
Product ID
0781-5274_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
5 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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0781-5274-10EA - Each0781-5274bd6156d5-8dd2-4c06-ac45-513f02dcca8912012-07-24
0781-5274-13EA - Each0781-5274e589492a-c647-4916-ac7f-170e2484533c12012-07-24
0781-5274-31EA - Each0781-52742e7245e0-a71f-4b3a-b64c-46ea533f9ebd12012-07-24
0781-5274-92EA - Each0781-5274a59b0cfa-63e1-4157-b0f0-39e162ca04e412012-07-24