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
62756-194-83	62756-194	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20150617	N/A	ANDA	ANDA204293	Sun Pharmaceutical Industries, Inc.	DONEPEZIL HYDROCHLORIDE	23 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62756-194-83)
62756-194-81	62756-194	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20150617	N/A	ANDA	ANDA204293	Sun Pharmaceutical Industries, Inc.	DONEPEZIL HYDROCHLORIDE	23 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62756-194-81)
62756-194-18	62756-194	HUMAN PRESCRIPTION DRUG	Donepezil Hydrochloride	Donepezil Hydrochloride	TABLET, FILM COATED	ORAL	20150617	N/A	ANDA	ANDA204293	Sun Pharmaceutical Industries, Inc.	DONEPEZIL HYDROCHLORIDE	23 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62756-194-18)