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
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)
68788-8208-3	68788-8208	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20220603	N/A	ANDA	ANDA090056	Preferred Pharmaceuticals Inc.	DONEPEZIL HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-8208-3)
68788-8208-6	68788-8208	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20220603	N/A	ANDA	ANDA090056	Preferred Pharmaceuticals Inc.	DONEPEZIL HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-8208-6)
68788-8208-9	68788-8208	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20220603	N/A	ANDA	ANDA090056	Preferred Pharmaceuticals Inc.	DONEPEZIL HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-8208-9)
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)
71335-2093-1	71335-2093	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA090056	Bryant Ranch Prepack	DONEPEZIL HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2093-1)
71335-2093-2	71335-2093	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20220506	N/A	ANDA	ANDA090056	Bryant Ranch Prepack	DONEPEZIL HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2093-2)
71335-2093-3	71335-2093	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA090056	Bryant Ranch Prepack	DONEPEZIL HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2093-3)
71335-2346-1	71335-2346	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20240206	N/A	ANDA	ANDA090056	Bryant Ranch Prepack	DONEPEZIL HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2346-1)
71335-2346-2	71335-2346	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20240206	N/A	ANDA	ANDA090056	Bryant Ranch Prepack	DONEPEZIL HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2346-2)
71335-2346-3	71335-2346	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20240206	N/A	ANDA	ANDA090056	Bryant Ranch Prepack	DONEPEZIL HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2346-3)