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
60687-213-94	60687-213	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20250801	N/A	ANDA	ANDA205064	American Health Packaging	ARIPIPRAZOLE	30 mg/1	20 BLISTER PACK in 1 CARTON (60687-213-94) / 1 TABLET in 1 BLISTER PACK (60687-213-11)
72789-462-14	72789-462	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20241223	N/A	ANDA	ANDA205064	PD-Rx Pharmaceuticals, Inc.	ARIPIPRAZOLE	5 mg/1	14 TABLET in 1 BOTTLE, PLASTIC (72789-462-14)
31722-819-01	31722-819	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20150428	N/A	ANDA	ANDA205064	Camber Pharmaceuticals, Inc.	ARIPIPRAZOLE	2 mg/1	100 TABLET in 1 BOTTLE (31722-819-01)
31722-819-05	31722-819	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20240202	N/A	ANDA	ANDA205064	Camber Pharmaceuticals, Inc.	ARIPIPRAZOLE	2 mg/1	500 TABLET in 1 BOTTLE (31722-819-05)
31722-819-30	31722-819	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20150428	N/A	ANDA	ANDA205064	Camber Pharmaceuticals, Inc.	ARIPIPRAZOLE	2 mg/1	30 TABLET in 1 BOTTLE (31722-819-30)
31722-819-31	31722-819	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20150428	N/A	ANDA	ANDA205064	Camber Pharmaceuticals, Inc.	ARIPIPRAZOLE	2 mg/1	10 TABLET in 1 BLISTER PACK (31722-819-31)
31722-819-32	31722-819	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20150428	N/A	ANDA	ANDA205064	Camber Pharmaceuticals, Inc.	ARIPIPRAZOLE	2 mg/1	250 TABLET in 1 CARTON (31722-819-32)
16714-141-01	16714-141	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20201001	N/A	ANDA	ANDA205064	NorthStar RxLLC	ARIPIPRAZOLE	2 mg/1	30 TABLET in 1 BOTTLE (16714-141-01)
16714-142-01	16714-142	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20201001	N/A	ANDA	ANDA205064	NorthStar RxLLC	ARIPIPRAZOLE	5 mg/1	30 TABLET in 1 BOTTLE (16714-142-01)
16714-143-01	16714-143	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20201001	N/A	ANDA	ANDA205064	NorthStar RxLLC	ARIPIPRAZOLE	10 mg/1	30 TABLET in 1 BOTTLE (16714-143-01)
16714-144-01	16714-144	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20201001	N/A	ANDA	ANDA205064	NorthStar RxLLC	ARIPIPRAZOLE	15 mg/1	30 TABLET in 1 BOTTLE (16714-144-01)
16714-145-01	16714-145	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20201001	N/A	ANDA	ANDA205064	NorthStar RxLLC	ARIPIPRAZOLE	20 mg/1	30 TABLET in 1 BOTTLE (16714-145-01)
16714-146-01	16714-146	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20201001	N/A	ANDA	ANDA205064	NorthStar RxLLC	ARIPIPRAZOLE	30 mg/1	30 TABLET in 1 BOTTLE (16714-146-01)
31722-820-01	31722-820	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20150428	N/A	ANDA	ANDA205064	Camber Pharmaceuticals, Inc.	ARIPIPRAZOLE	5 mg/1	100 TABLET in 1 BOTTLE (31722-820-01)
31722-820-05	31722-820	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20240202	N/A	ANDA	ANDA205064	Camber Pharmaceuticals, Inc.	ARIPIPRAZOLE	5 mg/1	500 TABLET in 1 BOTTLE (31722-820-05)
31722-820-30	31722-820	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20150428	N/A	ANDA	ANDA205064	Camber Pharmaceuticals, Inc.	ARIPIPRAZOLE	5 mg/1	30 TABLET in 1 BOTTLE (31722-820-30)
31722-820-31	31722-820	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20150428	N/A	ANDA	ANDA205064	Camber Pharmaceuticals, Inc.	ARIPIPRAZOLE	5 mg/1	10 TABLET in 1 BLISTER PACK (31722-820-31)
31722-820-32	31722-820	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20150428	N/A	ANDA	ANDA205064	Camber Pharmaceuticals, Inc.	ARIPIPRAZOLE	5 mg/1	250 TABLET in 1 CARTON (31722-820-32)
31722-827-01	31722-827	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20150428	N/A	ANDA	ANDA205064	Camber Pharmaceuticals, Inc.	ARIPIPRAZOLE	10 mg/1	100 TABLET in 1 BOTTLE (31722-827-01)
31722-827-05	31722-827	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20240202	N/A	ANDA	ANDA205064	Camber Pharmaceuticals, Inc.	ARIPIPRAZOLE	10 mg/1	500 TABLET in 1 BOTTLE (31722-827-05)