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
60505-2676-3	60505-2676	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20150724	20241231	ANDA	ANDA078583	Apotex Corp	ARIPIPRAZOLE	20 mg/1	30 TABLET in 1 BOTTLE (60505-2676-3)
60505-2676-8	60505-2676	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20150724	20241231	ANDA	ANDA078583	Apotex Corp	ARIPIPRAZOLE	20 mg/1	1000 TABLET in 1 BOTTLE (60505-2676-8)
60505-3075-3	60505-3075	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20150724	20241231	ANDA	ANDA078583	Apotex Corp	ARIPIPRAZOLE	2 mg/1	30 TABLET in 1 BOTTLE (60505-3075-3)
60505-3075-8	60505-3075	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20150724	20241231	ANDA	ANDA078583	Apotex Corp	ARIPIPRAZOLE	2 mg/1	1000 TABLET in 1 BOTTLE (60505-3075-8)
71335-2263-1	71335-2263	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20231013	20241231	ANDA	ANDA078583	Bryant Ranch Prepack	ARIPIPRAZOLE	20 mg/1	30 TABLET in 1 BOTTLE (71335-2263-1)
71335-2263-2	71335-2263	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20240403	20241231	ANDA	ANDA078583	Bryant Ranch Prepack	ARIPIPRAZOLE	20 mg/1	28 TABLET in 1 BOTTLE (71335-2263-2)
71335-2263-3	71335-2263	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20240403	20241231	ANDA	ANDA078583	Bryant Ranch Prepack	ARIPIPRAZOLE	20 mg/1	90 TABLET in 1 BOTTLE (71335-2263-3)