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
71205-439-90	71205-439	HUMAN PRESCRIPTION DRUG	celecoxib	celecoxib	CAPSULE	ORAL	20200319	N/A	ANDA	ANDA204590	Proficient Rx LP	CELECOXIB	100 mg/1	90 CAPSULE in 1 BOTTLE (71205-439-90)
76420-009-07	76420-009	HUMAN PRESCRIPTION DRUG	celecoxib	celecoxib	CAPSULE	ORAL	20200118	N/A	ANDA	ANDA204590	Asclemed USA, Inc.	CELECOXIB	200 mg/1	7 CAPSULE in 1 BOTTLE (76420-009-07)
76420-009-30	76420-009	HUMAN PRESCRIPTION DRUG	celecoxib	celecoxib	CAPSULE	ORAL	20200118	N/A	ANDA	ANDA204590	Asclemed USA, Inc.	CELECOXIB	200 mg/1	30 CAPSULE in 1 BOTTLE (76420-009-30)
76420-009-60	76420-009	HUMAN PRESCRIPTION DRUG	celecoxib	celecoxib	CAPSULE	ORAL	20200604	N/A	ANDA	ANDA204590	Asclemed USA, Inc.	CELECOXIB	200 mg/1	60 CAPSULE in 1 BOTTLE (76420-009-60)
76420-009-90	76420-009	HUMAN PRESCRIPTION DRUG	celecoxib	celecoxib	CAPSULE	ORAL	20230902	N/A	ANDA	ANDA204590	Asclemed USA, Inc.	CELECOXIB	200 mg/1	90 CAPSULE in 1 BOTTLE (76420-009-90)
76420-009-14	76420-009	HUMAN PRESCRIPTION DRUG	celecoxib	celecoxib	CAPSULE	ORAL	20230902	N/A	ANDA	ANDA204590	Asclemed USA, Inc.	CELECOXIB	200 mg/1	14 CAPSULE in 1 BOTTLE (76420-009-14)
76420-009-20	76420-009	HUMAN PRESCRIPTION DRUG	celecoxib	celecoxib	CAPSULE	ORAL	20230902	N/A	ANDA	ANDA204590	Asclemed USA, Inc.	CELECOXIB	200 mg/1	20 CAPSULE in 1 BOTTLE (76420-009-20)
76420-009-01	76420-009	HUMAN PRESCRIPTION DRUG	celecoxib	celecoxib	CAPSULE	ORAL	20200118	N/A	ANDA	ANDA204590	Asclemed USA, Inc.	CELECOXIB	200 mg/1	1 CAPSULE in 1 BOTTLE (76420-009-01)