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
59651-843-01	59651-843	HUMAN PRESCRIPTION DRUG	DICLOFENAC SODIUM	DICLOFENAC SODIUM	TABLET, DELAYED RELEASE	ORAL	20250417	N/A	ANDA	ANDA075281	Aurobindo Pharma Limited	DICLOFENAC SODIUM	75 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (59651-843-01)
59651-843-05	59651-843	HUMAN PRESCRIPTION DRUG	DICLOFENAC SODIUM	DICLOFENAC SODIUM	TABLET, DELAYED RELEASE	ORAL	20250417	N/A	ANDA	ANDA075281	Aurobindo Pharma Limited	DICLOFENAC SODIUM	75 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (59651-843-05)
59651-843-60	59651-843	HUMAN PRESCRIPTION DRUG	DICLOFENAC SODIUM	DICLOFENAC SODIUM	TABLET, DELAYED RELEASE	ORAL	20250417	N/A	ANDA	ANDA075281	Aurobindo Pharma Limited	DICLOFENAC SODIUM	75 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (59651-843-60)
59651-843-99	59651-843	HUMAN PRESCRIPTION DRUG	DICLOFENAC SODIUM	DICLOFENAC SODIUM	TABLET, DELAYED RELEASE	ORAL	20250417	N/A	ANDA	ANDA075281	Aurobindo Pharma Limited	DICLOFENAC SODIUM	75 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (59651-843-99)
59651-842-01	59651-842	HUMAN PRESCRIPTION DRUG	DICLOFENAC SODIUM	DICLOFENAC SODIUM	TABLET, DELAYED RELEASE	ORAL	20250417	N/A	ANDA	ANDA075281	Aurobindo Pharma Limited	DICLOFENAC SODIUM	50 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (59651-842-01)
59651-842-60	59651-842	HUMAN PRESCRIPTION DRUG	DICLOFENAC SODIUM	DICLOFENAC SODIUM	TABLET, DELAYED RELEASE	ORAL	20250417	N/A	ANDA	ANDA075281	Aurobindo Pharma Limited	DICLOFENAC SODIUM	50 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (59651-842-60)
59651-842-99	59651-842	HUMAN PRESCRIPTION DRUG	DICLOFENAC SODIUM	DICLOFENAC SODIUM	TABLET, DELAYED RELEASE	ORAL	20250417	N/A	ANDA	ANDA075281	Aurobindo Pharma Limited	DICLOFENAC SODIUM	50 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (59651-842-99)