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
71209-056-05	71209-056	HUMAN PRESCRIPTION DRUG	Celecoxib	Celecoxib	CAPSULE	ORAL	20210910	N/A	ANDA	ANDA208701	Cadila Pharmaceuticals Limited	CELECOXIB	200 mg/1	100 CAPSULE in 1 BOTTLE (71209-056-05)
71209-056-10	71209-056	HUMAN PRESCRIPTION DRUG	Celecoxib	Celecoxib	CAPSULE	ORAL	20210910	N/A	ANDA	ANDA208701	Cadila Pharmaceuticals Limited	CELECOXIB	200 mg/1	500 CAPSULE in 1 BOTTLE (71209-056-10)
71209-056-11	71209-056	HUMAN PRESCRIPTION DRUG	Celecoxib	Celecoxib	CAPSULE	ORAL	20180823	N/A	ANDA	ANDA208701	Cadila Pharmaceuticals Limited	CELECOXIB	200 mg/1	1000 CAPSULE in 1 BOTTLE (71209-056-11)
71209-057-03	71209-057	HUMAN PRESCRIPTION DRUG	Celecoxib	Celecoxib	CAPSULE	ORAL	20180823	N/A	ANDA	ANDA208701	Cadila Pharmaceuticals Limited	CELECOXIB	400 mg/1	60 CAPSULE in 1 BOTTLE (71209-057-03)
71209-057-20	71209-057	HUMAN PRESCRIPTION DRUG	Celecoxib	Celecoxib	CAPSULE	ORAL	20180823	N/A	ANDA	ANDA208701	Cadila Pharmaceuticals Limited	CELECOXIB	400 mg/1	600 CAPSULE in 1 BOTTLE (71209-057-20)
72241-025-20	72241-025	HUMAN PRESCRIPTION DRUG	Celecoxib	Celecoxib	CAPSULE	ORAL	20210823	N/A	ANDA	ANDA208701	Modavar Pharmaceuticals LLC	CELECOXIB	400 mg/1	600 CAPSULE in 1 BOTTLE (72241-025-20)
71209-054-03	71209-054	HUMAN PRESCRIPTION DRUG	Celecoxib	Celecoxib	CAPSULE	ORAL	20180823	N/A	ANDA	ANDA208701	Cadila Pharmaceuticals Limited	CELECOXIB	50 mg/1	60 CAPSULE in 1 BOTTLE (71209-054-03)
71209-054-11	71209-054	HUMAN PRESCRIPTION DRUG	Celecoxib	Celecoxib	CAPSULE	ORAL	20180823	N/A	ANDA	ANDA208701	Cadila Pharmaceuticals Limited	CELECOXIB	50 mg/1	1000 CAPSULE in 1 BOTTLE (71209-054-11)