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
55111-302-90	55111-302	HUMAN PRESCRIPTION DRUG	Donepezil hydrochloride	Donepezil hydrochloride	TABLET, FILM COATED	ORAL	20130726	N/A	ANDA	ANDA202723	Dr. Reddys Laboratories Limited	DONEPEZIL HYDROCHLORIDE	23 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (55111-302-90)
55111-302-30	55111-302	HUMAN PRESCRIPTION DRUG	Donepezil hydrochloride	Donepezil hydrochloride	TABLET, FILM COATED	ORAL	20130726	N/A	ANDA	ANDA202723	Dr. Reddys Laboratories Limited	DONEPEZIL HYDROCHLORIDE	23 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (55111-302-30)
55111-302-10	55111-302	HUMAN PRESCRIPTION DRUG	Donepezil hydrochloride	Donepezil hydrochloride	TABLET, FILM COATED	ORAL	20130726	N/A	ANDA	ANDA202723	Dr. Reddys Laboratories Limited	DONEPEZIL HYDROCHLORIDE	23 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (55111-302-10)
55111-302-05	55111-302	HUMAN PRESCRIPTION DRUG	Donepezil hydrochloride	Donepezil hydrochloride	TABLET, FILM COATED	ORAL	20130726	N/A	ANDA	ANDA202723	Dr. Reddys Laboratories Limited	DONEPEZIL HYDROCHLORIDE	23 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (55111-302-05)