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
71335-0868-7	71335-0868	HUMAN PRESCRIPTION DRUG	celecoxib	celecoxib	CAPSULE	ORAL	20180705	N/A	ANDA	ANDA204590	Bryant Ranch Prepack	CELECOXIB	200 mg/1	180 CAPSULE in 1 BOTTLE (71335-0868-7)
71335-0868-8	71335-0868	HUMAN PRESCRIPTION DRUG	celecoxib	celecoxib	CAPSULE	ORAL	20180705	N/A	ANDA	ANDA204590	Bryant Ranch Prepack	CELECOXIB	200 mg/1	28 CAPSULE in 1 BOTTLE (71335-0868-8)
71335-0868-9	71335-0868	HUMAN PRESCRIPTION DRUG	celecoxib	celecoxib	CAPSULE	ORAL	20180705	N/A	ANDA	ANDA204590	Bryant Ranch Prepack	CELECOXIB	200 mg/1	56 CAPSULE in 1 BOTTLE (71335-0868-9)
63739-298-10	63739-298	HUMAN PRESCRIPTION DRUG	celecoxib	celecoxib	CAPSULE	ORAL	20240627	20260430	ANDA	ANDA204590	McKesson Corporation dba SKY Packaging	CELECOXIB	200 mg/1	100 CAPSULE in 1 CARTON (63739-298-10)
67296-1399-6	67296-1399	HUMAN PRESCRIPTION DRUG	celecoxib	celecoxib	CAPSULE	ORAL	20210101	N/A	ANDA	ANDA204590	RedPharm Drug, Inc.	CELECOXIB	200 mg/1	60 CAPSULE in 1 BOTTLE (67296-1399-6)
68071-4392-3	68071-4392	HUMAN PRESCRIPTION DRUG	celecoxib	celecoxib	CAPSULE	ORAL	20180412	N/A	ANDA	ANDA204590	NuCare Pharmaceuticals,Inc.	CELECOXIB	200 mg/1	30 CAPSULE in 1 BOTTLE (68071-4392-3)
68071-4392-7	68071-4392	HUMAN PRESCRIPTION DRUG	celecoxib	celecoxib	CAPSULE	ORAL	20180412	N/A	ANDA	ANDA204590	NuCare Pharmaceuticals,Inc.	CELECOXIB	200 mg/1	7 CAPSULE in 1 BOTTLE (68071-4392-7)