FDA.reportPublic FDA data

Application 202415

Type
ANDA
Sponsor
ACTAVIS ELIZABETH

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001DONEPEZIL HYDROCHLORIDEDONEPEZIL HYDROCHLORIDETABLET;ORAL23MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0228-4529Donepezil hydrochlorideDonepezil hydrochlorideActavis Pharma, Inc.ANDACurrent
0228-4529Donepezil hydrochlorideDonepezil hydrochlorideActavis Pharma, Inc.ANDACurrent
0228-4529Donepezil hydrochlorideDonepezil hydrochlorideActavis Pharma, Inc.ANDACurrent
0228-4529Donepezil hydrochlorideDonepezil hydrochlorideActavis Pharma, Inc.ANDACurrent
0228-4529Donepezil hydrochlorideDonepezil hydrochlorideActavis Pharma, Inc.ANDACurrent