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
72162-1355-3	72162-1355	HUMAN PRESCRIPTION DRUG	donepezil hydrochloride	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20240201	N/A	ANDA	ANDA203713	Bryant Ranch Prepack	DONEPEZIL HYDROCHLORIDE	23 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72162-1355-3)
72162-1355-9	72162-1355	HUMAN PRESCRIPTION DRUG	donepezil hydrochloride	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20240201	N/A	ANDA	ANDA203713	Bryant Ranch Prepack	DONEPEZIL HYDROCHLORIDE	23 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72162-1355-9)
63629-1117-1	63629-1117	HUMAN PRESCRIPTION DRUG	donepezil hydrochloride	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20161205	N/A	ANDA	ANDA203713	Bryant Ranch Prepack	DONEPEZIL HYDROCHLORIDE	23 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63629-1117-1)
63629-1118-1	63629-1118	HUMAN PRESCRIPTION DRUG	donepezil hydrochloride	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20200730	N/A	ANDA	ANDA203713	Bryant Ranch Prepack	DONEPEZIL HYDROCHLORIDE	23 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63629-1118-1)
42799-954-01	42799-954	HUMAN PRESCRIPTION DRUG	Donepezil hydrochloride	Donepezil hydrochloride	TABLET, FILM COATED	ORAL	20231205	N/A	ANDA	ANDA203713	Edenbridge Pharmaceuticals LLC.	DONEPEZIL HYDROCHLORIDE	23 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42799-954-01)
42799-954-02	42799-954	HUMAN PRESCRIPTION DRUG	Donepezil hydrochloride	Donepezil hydrochloride	TABLET, FILM COATED	ORAL	20231205	N/A	ANDA	ANDA203713	Edenbridge Pharmaceuticals LLC.	DONEPEZIL HYDROCHLORIDE	23 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (42799-954-02)