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
50090-6927-0	50090-6927	HUMAN PRESCRIPTION DRUG	Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20231214	N/A	ANDA	ANDA210086	A-S Medication Solutions	AMITRIPTYLINE HYDROCHLORIDE	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6927-0)
70710-1225-0	70710-1225	HUMAN PRESCRIPTION DRUG	Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20171226	N/A	ANDA	ANDA210086	Zydus Pharmaceuticals USA Inc.	AMITRIPTYLINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70710-1225-0)
70710-1225-1	70710-1225	HUMAN PRESCRIPTION DRUG	Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20171226	N/A	ANDA	ANDA210086	Zydus Pharmaceuticals USA Inc.	AMITRIPTYLINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70710-1225-1)
50090-7183-0	50090-7183	HUMAN PRESCRIPTION DRUG	Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20240618	N/A	ANDA	ANDA210086	A-S Medication Solutions	AMITRIPTYLINE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (50090-7183-0)
50090-7183-1	50090-7183	HUMAN PRESCRIPTION DRUG	Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20240618	N/A	ANDA	ANDA210086	A-S Medication Solutions	AMITRIPTYLINE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-7183-1)
50090-7183-2	50090-7183	HUMAN PRESCRIPTION DRUG	Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20240618	N/A	ANDA	ANDA210086	A-S Medication Solutions	AMITRIPTYLINE HYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-7183-2)
70710-1229-0	70710-1229	HUMAN PRESCRIPTION DRUG	Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20171226	N/A	ANDA	ANDA210086	Zydus Pharmaceuticals USA Inc.	AMITRIPTYLINE HYDROCHLORIDE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70710-1229-0)
70710-1229-1	70710-1229	HUMAN PRESCRIPTION DRUG	Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20171226	N/A	ANDA	ANDA210086	Zydus Pharmaceuticals USA Inc.	AMITRIPTYLINE HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70710-1229-1)
50090-7183-5	50090-7183	HUMAN PRESCRIPTION DRUG	Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	TABLET, FILM COATED	ORAL	20240618	N/A	ANDA	ANDA210086	A-S Medication Solutions	AMITRIPTYLINE HYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7183-5)