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
68382-521-10	68382-521	HUMAN PRESCRIPTION DRUG	donepezil hydrochloride	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20180307	N/A	ANDA	ANDA203162	Zydus Pharmaceuticals USA Inc.	DONEPEZIL HYDROCHLORIDE	23 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-521-10)
68382-521-16	68382-521	HUMAN PRESCRIPTION DRUG	donepezil hydrochloride	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20180307	N/A	ANDA	ANDA203162	Zydus Pharmaceuticals USA Inc.	DONEPEZIL HYDROCHLORIDE	23 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-521-16)
68382-521-77	68382-521	HUMAN PRESCRIPTION DRUG	donepezil hydrochloride	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20180307	N/A	ANDA	ANDA203162	Zydus Pharmaceuticals USA Inc.	DONEPEZIL HYDROCHLORIDE	23 mg/1	10 BLISTER PACK in 1 CARTON (68382-521-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-521-30)
68382-521-06	68382-521	HUMAN PRESCRIPTION DRUG	donepezil hydrochloride	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20180307	N/A	ANDA	ANDA203162	Zydus Pharmaceuticals USA Inc.	DONEPEZIL HYDROCHLORIDE	23 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-521-06)
68382-521-05	68382-521	HUMAN PRESCRIPTION DRUG	donepezil hydrochloride	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20180307	N/A	ANDA	ANDA203162	Zydus Pharmaceuticals USA Inc.	DONEPEZIL HYDROCHLORIDE	23 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68382-521-05)
68382-521-01	68382-521	HUMAN PRESCRIPTION DRUG	donepezil hydrochloride	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20180307	N/A	ANDA	ANDA203162	Zydus Pharmaceuticals USA Inc.	DONEPEZIL HYDROCHLORIDE	23 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-521-01)
70771-1320-0	70771-1320	HUMAN PRESCRIPTION DRUG	donepezil hydrochloride	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20180307	N/A	ANDA	ANDA203162	Zydus Lifesciences Limited	DONEPEZIL HYDROCHLORIDE	23 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70771-1320-0)
70771-1320-5	70771-1320	HUMAN PRESCRIPTION DRUG	donepezil hydrochloride	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20180307	N/A	ANDA	ANDA203162	Zydus Lifesciences Limited	DONEPEZIL HYDROCHLORIDE	23 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (70771-1320-5)
70771-1320-9	70771-1320	HUMAN PRESCRIPTION DRUG	donepezil hydrochloride	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20180307	N/A	ANDA	ANDA203162	Zydus Lifesciences Limited	DONEPEZIL HYDROCHLORIDE	23 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1320-9)
70771-1320-1	70771-1320	HUMAN PRESCRIPTION DRUG	donepezil hydrochloride	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20180307	N/A	ANDA	ANDA203162	Zydus Lifesciences Limited	DONEPEZIL HYDROCHLORIDE	23 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1320-1)
70771-1320-3	70771-1320	HUMAN PRESCRIPTION DRUG	donepezil hydrochloride	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20180307	N/A	ANDA	ANDA203162	Zydus Lifesciences Limited	DONEPEZIL HYDROCHLORIDE	23 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1320-3)
70771-1320-4	70771-1320	HUMAN PRESCRIPTION DRUG	donepezil hydrochloride	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20180307	N/A	ANDA	ANDA203162	Zydus Lifesciences Limited	DONEPEZIL HYDROCHLORIDE	23 mg/1	10 BLISTER PACK in 1 CARTON (70771-1320-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1320-2)