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
67877-435-03	67877-435	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20190227	N/A	ANDA	ANDA207105	Ascend Laboratories, LLC	ARIPIPRAZOLE	30 mg/1	30 TABLET in 1 BOTTLE (67877-435-03)
67877-435-05	67877-435	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20190227	N/A	ANDA	ANDA207105	Ascend Laboratories, LLC	ARIPIPRAZOLE	30 mg/1	500 TABLET in 1 BOTTLE (67877-435-05)
67877-435-38	67877-435	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20190227	N/A	ANDA	ANDA207105	Ascend Laboratories, LLC	ARIPIPRAZOLE	30 mg/1	10 BLISTER PACK in 1 CARTON (67877-435-38) / 10 TABLET in 1 BLISTER PACK (67877-435-33)
71335-1687-1	71335-1687	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20200804	N/A	ANDA	ANDA207105	Bryant Ranch Prepack	ARIPIPRAZOLE	20 mg/1	30 TABLET in 1 BOTTLE (71335-1687-1)
71335-1687-2	71335-1687	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20240404	N/A	ANDA	ANDA207105	Bryant Ranch Prepack	ARIPIPRAZOLE	20 mg/1	28 TABLET in 1 BOTTLE (71335-1687-2)
71335-1687-3	71335-1687	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20240404	N/A	ANDA	ANDA207105	Bryant Ranch Prepack	ARIPIPRAZOLE	20 mg/1	90 TABLET in 1 BOTTLE (71335-1687-3)
68788-8089-6	68788-8089	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20211005	N/A	ANDA	ANDA207105	Preferred Pharmaceuticals Inc.	ARIPIPRAZOLE	5 mg/1	60 TABLET in 1 BOTTLE (68788-8089-6)
68788-8089-9	68788-8089	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20211005	N/A	ANDA	ANDA207105	Preferred Pharmaceuticals Inc.	ARIPIPRAZOLE	5 mg/1	90 TABLET in 1 BOTTLE (68788-8089-9)