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
65162-818-10	65162-818	HUMAN PRESCRIPTION DRUG	Celecoxib	Celecoxib	CAPSULE	ORAL	20180625	N/A	ANDA	ANDA208833	Amneal Pharmaceuticals LLC	CELECOXIB	100 mg/1	100 CAPSULE in 1 BOTTLE (65162-818-10)
65162-818-11	65162-818	HUMAN PRESCRIPTION DRUG	Celecoxib	Celecoxib	CAPSULE	ORAL	20180625	N/A	ANDA	ANDA208833	Amneal Pharmaceuticals LLC	CELECOXIB	100 mg/1	1000 CAPSULE in 1 BOTTLE (65162-818-11)
65162-818-50	65162-818	HUMAN PRESCRIPTION DRUG	Celecoxib	Celecoxib	CAPSULE	ORAL	20180625	N/A	ANDA	ANDA208833	Amneal Pharmaceuticals LLC	CELECOXIB	100 mg/1	500 CAPSULE in 1 BOTTLE (65162-818-50)
65162-819-10	65162-819	HUMAN PRESCRIPTION DRUG	Celecoxib	Celecoxib	CAPSULE	ORAL	20180625	N/A	ANDA	ANDA208833	Amneal Pharmaceuticals LLC	CELECOXIB	200 mg/1	100 CAPSULE in 1 BOTTLE (65162-819-10)
65162-819-11	65162-819	HUMAN PRESCRIPTION DRUG	Celecoxib	Celecoxib	CAPSULE	ORAL	20180625	N/A	ANDA	ANDA208833	Amneal Pharmaceuticals LLC	CELECOXIB	200 mg/1	1000 CAPSULE in 1 BOTTLE (65162-819-11)
65162-819-50	65162-819	HUMAN PRESCRIPTION DRUG	Celecoxib	Celecoxib	CAPSULE	ORAL	20180625	N/A	ANDA	ANDA208833	Amneal Pharmaceuticals LLC	CELECOXIB	200 mg/1	500 CAPSULE in 1 BOTTLE (65162-819-50)
65162-817-06	65162-817	HUMAN PRESCRIPTION DRUG	Celecoxib	Celecoxib	CAPSULE	ORAL	20180625	N/A	ANDA	ANDA208833	Amneal Pharmaceuticals LLC	CELECOXIB	50 mg/1	60 CAPSULE in 1 BOTTLE (65162-817-06)
65162-820-06	65162-820	HUMAN PRESCRIPTION DRUG	Celecoxib	Celecoxib	CAPSULE	ORAL	20180625	N/A	ANDA	ANDA208833	Amneal Pharmaceuticals LLC	CELECOXIB	400 mg/1	60 CAPSULE in 1 BOTTLE (65162-820-06)