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
82619-106-01	82619-106	HUMAN PRESCRIPTION DRUG	HALOPERIDOL	haloperidol	TABLET	ORAL	20260105	N/A	ANDA	ANDA218162	Creekwood Pharmaceuticals LLC	HALOPERIDOL	1 mg/1	100 TABLET in 1 BOTTLE (82619-106-01)
82619-106-02	82619-106	HUMAN PRESCRIPTION DRUG	HALOPERIDOL	haloperidol	TABLET	ORAL	20260105	N/A	ANDA	ANDA218162	Creekwood Pharmaceuticals LLC	HALOPERIDOL	1 mg/1	1000 TABLET in 1 BOTTLE (82619-106-02)
82619-107-01	82619-107	HUMAN PRESCRIPTION DRUG	HALOPERIDOL	haloperidol	TABLET	ORAL	20260105	N/A	ANDA	ANDA218162	Creekwood Pharmaceuticals LLC	HALOPERIDOL	2 mg/1	100 TABLET in 1 BOTTLE (82619-107-01)
82619-107-02	82619-107	HUMAN PRESCRIPTION DRUG	HALOPERIDOL	haloperidol	TABLET	ORAL	20260105	N/A	ANDA	ANDA218162	Creekwood Pharmaceuticals LLC	HALOPERIDOL	2 mg/1	1000 TABLET in 1 BOTTLE (82619-107-02)
82619-108-01	82619-108	HUMAN PRESCRIPTION DRUG	HALOPERIDOL	haloperidol	TABLET	ORAL	20260105	N/A	ANDA	ANDA218162	Creekwood Pharmaceuticals LLC	HALOPERIDOL	5 mg/1	30 TABLET in 1 BOTTLE (82619-108-01)
82619-108-02	82619-108	HUMAN PRESCRIPTION DRUG	HALOPERIDOL	haloperidol	TABLET	ORAL	20260105	N/A	ANDA	ANDA218162	Creekwood Pharmaceuticals LLC	HALOPERIDOL	5 mg/1	100 TABLET in 1 BOTTLE (82619-108-02)
82619-108-03	82619-108	HUMAN PRESCRIPTION DRUG	HALOPERIDOL	haloperidol	TABLET	ORAL	20260105	N/A	ANDA	ANDA218162	Creekwood Pharmaceuticals LLC	HALOPERIDOL	5 mg/1	1000 TABLET in 1 BOTTLE (82619-108-03)
82619-109-01	82619-109	HUMAN PRESCRIPTION DRUG	HALOPERIDOL	haloperidol	TABLET	ORAL	20260105	N/A	ANDA	ANDA218162	Creekwood Pharmaceuticals LLC	HALOPERIDOL	10 mg/1	30 TABLET in 1 BOTTLE (82619-109-01)
82619-109-02	82619-109	HUMAN PRESCRIPTION DRUG	HALOPERIDOL	haloperidol	TABLET	ORAL	20260105	N/A	ANDA	ANDA218162	Creekwood Pharmaceuticals LLC	HALOPERIDOL	10 mg/1	100 TABLET in 1 BOTTLE (82619-109-02)
82619-109-03	82619-109	HUMAN PRESCRIPTION DRUG	HALOPERIDOL	haloperidol	TABLET	ORAL	20260105	N/A	ANDA	ANDA218162	Creekwood Pharmaceuticals LLC	HALOPERIDOL	10 mg/1	1000 TABLET in 1 BOTTLE (82619-109-03)
82619-110-01	82619-110	HUMAN PRESCRIPTION DRUG	HALOPERIDOL	haloperidol	TABLET	ORAL	20260105	N/A	ANDA	ANDA218162	Creekwood Pharmaceuticals LLC	HALOPERIDOL	20 mg/1	30 TABLET in 1 BOTTLE (82619-110-01)
82619-110-02	82619-110	HUMAN PRESCRIPTION DRUG	HALOPERIDOL	haloperidol	TABLET	ORAL	20260105	N/A	ANDA	ANDA218162	Creekwood Pharmaceuticals LLC	HALOPERIDOL	20 mg/1	100 TABLET in 1 BOTTLE (82619-110-02)
82619-105-02	82619-105	HUMAN PRESCRIPTION DRUG	HALOPERIDOL	haloperidol	TABLET	ORAL	20260105	N/A	ANDA	ANDA218162	Creekwood Pharmaceuticals LLC	HALOPERIDOL	.5 mg/1	1000 TABLET in 1 BOTTLE (82619-105-02)
82619-105-01	82619-105	HUMAN PRESCRIPTION DRUG	HALOPERIDOL	haloperidol	TABLET	ORAL	20260105	N/A	ANDA	ANDA218162	Creekwood Pharmaceuticals LLC	HALOPERIDOL	.5 mg/1	100 TABLET in 1 BOTTLE (82619-105-01)