donepezil hydrochloride

Product NDC
65841-750
11-digit product format
658410750
Labeler code
65841
Product ID
65841-750_3ca60c78-2542-4158-ab90-ad32d5271bd1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
donepezil hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Zydus Lifesciences Limited
Application
ANDA090100
Marketing category
ANDA
Marketing start
2011-05-25
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
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65841-750DONEPEZIL HYDROCHLORIDE TABLET, FILM COATED [ZYDUS LIFESCIENCES LIMITED]5Legacy NDC20221109_43a18848-fb43-4adb-9273-a3fe812e3d05.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
65841-750-0165841075001100 TABLET, FILM COATED in 1 BOTTLE (65841-750-01) 2011-05-250000-00-00NoNoCurrent
65841-750-0565841075005500 TABLET, FILM COATED in 1 BOTTLE (65841-750-05) 2011-05-250000-00-00NoNoCurrent
65841-750-066584107500630 TABLET, FILM COATED in 1 BOTTLE (65841-750-06) 2011-05-250000-00-00NoNoCurrent
65841-750-10658410750101000 TABLET, FILM COATED in 1 BOTTLE (65841-750-10) 2011-05-250000-00-00NoNoCurrent
65841-750-166584107501690 TABLET, FILM COATED in 1 BOTTLE (65841-750-16) 2011-05-250000-00-00NoNoCurrent
65841-750-306584107503010 BLISTER PACK in 1 CARTON (65841-750-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK10 blister pack2011-05-250000-00-00NoNoCurrent