美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
33342-028-44	33342-028	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20141106	N/A	ANDA	ANDA201146	Macleods Pharmaceuticals Limited	DONEPEZIL HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (33342-028-44)
71335-0416-1	71335-0416	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20200724	N/A	ANDA	ANDA201146	Bryant Ranch Prepack	DONEPEZIL HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0416-1)
71335-0416-2	71335-0416	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA201146	Bryant Ranch Prepack	DONEPEZIL HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0416-2)
71335-0416-3	71335-0416	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20211222	N/A	ANDA	ANDA201146	Bryant Ranch Prepack	DONEPEZIL HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0416-3)
0615-7951-05	0615-7951	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20120817	N/A	ANDA	ANDA201146	NCS HealthCare of KY, LLC dba Vangard Labs	DONEPEZIL HYDROCHLORIDE	5 mg/1	15 TABLET, FILM COATED in 1 BLISTER PACK (0615-7951-05)
0615-7951-39	0615-7951	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20120817	N/A	ANDA	ANDA201146	NCS HealthCare of KY, LLC dba Vangard Labs	DONEPEZIL HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7951-39)