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
60687-799-17	60687-799	HUMAN PRESCRIPTION DRUG	Haloperidol	Haloperidol	SOLUTION	ORAL	20240226	N/A	ANDA	ANDA073037	American Health Packaging	HALOPERIDOL	2 mg/mL	10 TRAY in 1 CASE (60687-799-17) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-799-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-799-40)
0121-0581-04	0121-0581	HUMAN PRESCRIPTION DRUG	Haloperidol	Haloperidol	SOLUTION	ORAL	20091110	N/A	ANDA	ANDA073037	PAI Holdings, LLC	HALOPERIDOL	2 mg/mL	120 mL in 1 BOTTLE (0121-0581-04)
0121-0581-05	0121-0581	HUMAN PRESCRIPTION DRUG	Haloperidol	Haloperidol	SOLUTION	ORAL	20091110	N/A	ANDA	ANDA073037	PAI Holdings, LLC	HALOPERIDOL	2 mg/mL	10 TRAY in 1 CASE (0121-0581-05) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE
0121-0581-15	0121-0581	HUMAN PRESCRIPTION DRUG	Haloperidol	Haloperidol	SOLUTION	ORAL	20200612	N/A	ANDA	ANDA073037	PAI Holdings, LLC	HALOPERIDOL	2 mg/mL	15 mL in 1 BOTTLE (0121-0581-15)