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
51672-4180-4	51672-4180	HUMAN PRESCRIPTION DRUG	Iloperidone	Iloperidone	TABLET	ORAL	20190722	N/A	ANDA	ANDA207098	Taro Pharmaceuticals U.S.A., Inc.	ILOPERIDONE	4 mg/1	60 TABLET in 1 BOTTLE (51672-4180-4)
51672-4184-4	51672-4184	HUMAN PRESCRIPTION DRUG	Iloperidone	Iloperidone	TABLET	ORAL	20190722	N/A	ANDA	ANDA207098	Taro Pharmaceuticals U.S.A., Inc.	ILOPERIDONE	12 mg/1	60 TABLET in 1 BOTTLE (51672-4184-4)
51672-4179-4	51672-4179	HUMAN PRESCRIPTION DRUG	Iloperidone	Iloperidone	TABLET	ORAL	20190722	N/A	ANDA	ANDA207098	Taro Pharmaceuticals U.S.A., Inc.	ILOPERIDONE	2 mg/1	60 TABLET in 1 BOTTLE (51672-4179-4)
51672-4183-4	51672-4183	HUMAN PRESCRIPTION DRUG	Iloperidone	Iloperidone	TABLET	ORAL	20190722	N/A	ANDA	ANDA207098	Taro Pharmaceuticals U.S.A., Inc.	ILOPERIDONE	10 mg/1	60 TABLET in 1 BOTTLE (51672-4183-4)
51672-4178-4	51672-4178	HUMAN PRESCRIPTION DRUG	Iloperidone	Iloperidone	TABLET	ORAL	20190722	N/A	ANDA	ANDA207098	Taro Pharmaceuticals U.S.A., Inc.	ILOPERIDONE	1 mg/1	60 TABLET in 1 BOTTLE (51672-4178-4)
51672-4182-4	51672-4182	HUMAN PRESCRIPTION DRUG	Iloperidone	Iloperidone	TABLET	ORAL	20190722	N/A	ANDA	ANDA207098	Taro Pharmaceuticals U.S.A., Inc.	ILOPERIDONE	8 mg/1	60 TABLET in 1 BOTTLE (51672-4182-4)
51672-4213-7	51672-4213	HUMAN PRESCRIPTION DRUG	Iloperidone	Iloperidone	KIT		20190722	N/A	ANDA	ANDA207098	Taro Pharmaceuticals U.S.A., Inc.			1 BLISTER PACK in 1 DOSE PACK (51672-4213-7) / 1 KIT in 1 BLISTER PACK
51672-4181-4	51672-4181	HUMAN PRESCRIPTION DRUG	Iloperidone	Iloperidone	TABLET	ORAL	20190722	N/A	ANDA	ANDA207098	Taro Pharmaceuticals U.S.A., Inc.	ILOPERIDONE	6 mg/1	60 TABLET in 1 BOTTLE (51672-4181-4)