DONEPEZIL HYDROCHLORIDE

Product NDC
63187-401
11-digit product format
631870401
Labeler code
63187
Product ID
63187-401_531ec397-a99e-44f3-8c1f-52929a70359a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
DONEPEZIL HYDROCHLORIDE
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA090768
Marketing category
ANDA
Marketing start
2011-05-29
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
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63187-401DONEPEZIL HYDROCHLORIDE TABLET, FILM COATED [PROFICIENT RX LP]3Legacy NDC20210115_31d6a5a0-eaf0-4c7c-8d50-742ae520cca9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
63187-401-306318704013030 TABLET, FILM COATED in 1 BOTTLE (63187-401-30) 2019-01-010000-00-00NoNoCurrent