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
58151-083-01	58151-083	HUMAN PRESCRIPTION DRUG	CELEBREX	Celecoxib	CAPSULE	ORAL	20240913	N/A	NDA	NDA020998	Viatris Specialty LLC	CELECOXIB	100 mg/1	100 CAPSULE in 1 BOTTLE (58151-083-01)
58151-083-05	58151-083	HUMAN PRESCRIPTION DRUG	CELEBREX	Celecoxib	CAPSULE	ORAL	20240913	N/A	NDA	NDA020998	Viatris Specialty LLC	CELECOXIB	100 mg/1	500 CAPSULE in 1 BOTTLE (58151-083-05)
58151-083-88	58151-083	HUMAN PRESCRIPTION DRUG	CELEBREX	Celecoxib	CAPSULE	ORAL	20240917	N/A	NDA	NDA020998	Viatris Specialty LLC	CELECOXIB	100 mg/1	100 BLISTER PACK in 1 CARTON (58151-083-88) / 1 CAPSULE in 1 BLISTER PACK (58151-083-32)
58151-082-91	58151-082	HUMAN PRESCRIPTION DRUG	CELEBREX	Celecoxib	CAPSULE	ORAL	20231011	N/A	NDA	NDA020998	Viatris Specialty LLC	CELECOXIB	50 mg/1	60 CAPSULE in 1 BOTTLE (58151-082-91)
58151-084-01	58151-084	HUMAN PRESCRIPTION DRUG	CELEBREX	Celecoxib	CAPSULE	ORAL	20240110	N/A	NDA	NDA020998	Viatris Specialty LLC	CELECOXIB	200 mg/1	100 CAPSULE in 1 BOTTLE (58151-084-01)
58151-084-05	58151-084	HUMAN PRESCRIPTION DRUG	CELEBREX	Celecoxib	CAPSULE	ORAL	20240620	N/A	NDA	NDA020998	Viatris Specialty LLC	CELECOXIB	200 mg/1	500 CAPSULE in 1 BOTTLE (58151-084-05)
58151-084-88	58151-084	HUMAN PRESCRIPTION DRUG	CELEBREX	Celecoxib	CAPSULE	ORAL	20240830	N/A	NDA	NDA020998	Viatris Specialty LLC	CELECOXIB	200 mg/1	100 BLISTER PACK in 1 CARTON (58151-084-88) / 1 CAPSULE in 1 BLISTER PACK (58151-084-32)
58151-085-88	58151-085	HUMAN PRESCRIPTION DRUG	CELEBREX	Celecoxib	CAPSULE	ORAL	20231011	N/A	NDA	NDA020998	Viatris Specialty LLC	CELECOXIB	400 mg/1	100 BLISTER PACK in 1 CARTON (58151-085-88) / 1 CAPSULE in 1 BLISTER PACK (58151-085-32)
58151-085-91	58151-085	HUMAN PRESCRIPTION DRUG	CELEBREX	Celecoxib	CAPSULE	ORAL	20230912	N/A	NDA	NDA020998	Viatris Specialty LLC	CELECOXIB	400 mg/1	60 CAPSULE in 1 BOTTLE (58151-085-91)