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
67877-432-05	67877-432	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20190227	N/A	ANDA	ANDA207105	Ascend Laboratories, LLC	ARIPIPRAZOLE	10 mg/1	500 TABLET in 1 BOTTLE (67877-432-05)
67877-432-32	67877-432	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20190227	N/A	ANDA	ANDA207105	Ascend Laboratories, LLC	ARIPIPRAZOLE	10 mg/1	1 BLISTER PACK in 1 CARTON (67877-432-32) / 7 TABLET in 1 BLISTER PACK
67877-434-03	67877-434	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20190227	N/A	ANDA	ANDA207105	Ascend Laboratories, LLC	ARIPIPRAZOLE	20 mg/1	30 TABLET in 1 BOTTLE (67877-434-03)
67877-434-05	67877-434	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20190227	N/A	ANDA	ANDA207105	Ascend Laboratories, LLC	ARIPIPRAZOLE	20 mg/1	500 TABLET in 1 BOTTLE (67877-434-05)
67877-434-38	67877-434	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20190227	N/A	ANDA	ANDA207105	Ascend Laboratories, LLC	ARIPIPRAZOLE	20 mg/1	10 BLISTER PACK in 1 CARTON (67877-434-38) / 10 TABLET in 1 BLISTER PACK (67877-434-33)
67877-432-38	67877-432	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20190227	N/A	ANDA	ANDA207105	Ascend Laboratories, LLC	ARIPIPRAZOLE	10 mg/1	10 BLISTER PACK in 1 CARTON (67877-432-38) / 10 TABLET in 1 BLISTER PACK (67877-432-33)