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
65862-326-14	65862-326	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20110531	N/A	ANDA	ANDA090056	Aurobindo Pharma Limited	DONEPEZIL HYDROCHLORIDE	10 mg/1	10 BLISTER PACK in 1 CARTON (65862-326-14) / 14 TABLET, FILM COATED in 1 BLISTER PACK
65862-326-30	65862-326	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20110531	N/A	ANDA	ANDA090056	Aurobindo Pharma Limited	DONEPEZIL HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-326-30)
65862-326-90	65862-326	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20110531	N/A	ANDA	ANDA090056	Aurobindo Pharma Limited	DONEPEZIL HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-326-90)
65862-326-99	65862-326	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20110531	N/A	ANDA	ANDA090056	Aurobindo Pharma Limited	DONEPEZIL HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-326-99)
16571-778-03	16571-778	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20110531	N/A	ANDA	ANDA090056	Rising Pharma Holdings, Inc.	DONEPEZIL HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (16571-778-03)
16571-778-09	16571-778	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20110531	N/A	ANDA	ANDA090056	Rising Pharma Holdings, Inc.	DONEPEZIL HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (16571-778-09)
16571-778-10	16571-778	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20110531	N/A	ANDA	ANDA090056	Rising Pharma Holdings, Inc.	DONEPEZIL HYDROCHLORIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16571-778-10)
16571-778-50	16571-778	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20110531	N/A	ANDA	ANDA090056	Rising Pharma Holdings, Inc.	DONEPEZIL HYDROCHLORIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16571-778-50)
16571-779-03	16571-779	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20110531	N/A	ANDA	ANDA090056	Rising Pharma Holdings, Inc.	DONEPEZIL HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (16571-779-03)
16571-779-09	16571-779	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20110531	N/A	ANDA	ANDA090056	Rising Pharma Holdings, Inc.	DONEPEZIL HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (16571-779-09)
16571-779-10	16571-779	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20110531	N/A	ANDA	ANDA090056	Rising Pharma Holdings, Inc.	DONEPEZIL HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16571-779-10)
16571-779-50	16571-779	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20110531	N/A	ANDA	ANDA090056	Rising Pharma Holdings, Inc.	DONEPEZIL HYDROCHLORIDE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16571-779-50)
63629-9326-1	63629-9326	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20250605	N/A	ANDA	ANDA090056	Bryant Ranch Prepack	DONEPEZIL HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63629-9326-1)
63629-9326-2	63629-9326	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20250605	N/A	ANDA	ANDA090056	Bryant Ranch Prepack	DONEPEZIL HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63629-9326-2)
63629-9326-3	63629-9326	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20250605	N/A	ANDA	ANDA090056	Bryant Ranch Prepack	DONEPEZIL HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63629-9326-3)