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
67877-430-03	67877-430	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20190227	N/A	ANDA	ANDA207105	Ascend Laboratories, LLC	ARIPIPRAZOLE	2 mg/1	30 TABLET in 1 BOTTLE (67877-430-03)
67877-430-05	67877-430	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20190227	N/A	ANDA	ANDA207105	Ascend Laboratories, LLC	ARIPIPRAZOLE	2 mg/1	500 TABLET in 1 BOTTLE (67877-430-05)
72189-476-30	72189-476	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20230530	N/A	ANDA	ANDA207105	Direct_Rx	ARIPIPRAZOLE	10 mg/1	30 TABLET in 1 BOTTLE (72189-476-30)
67877-430-32	67877-430	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20190227	N/A	ANDA	ANDA207105	Ascend Laboratories, LLC	ARIPIPRAZOLE	2 mg/1	1 BLISTER PACK in 1 CARTON (67877-430-32) / 7 TABLET in 1 BLISTER PACK
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)