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
60290-082-01	60290-082	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20251124	N/A	ANDA	ANDA219945	Umedica Laboratories USA Inc.	DICLOFENAC SODIUM	25 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (60290-082-01)
60290-083-01	60290-083	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20251124	N/A	ANDA	ANDA219945	Umedica Laboratories USA Inc.	DICLOFENAC SODIUM	50 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (60290-083-01)
60290-083-02	60290-083	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20251124	N/A	ANDA	ANDA219945	Umedica Laboratories USA Inc.	DICLOFENAC SODIUM	50 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (60290-083-02)
60290-083-03	60290-083	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20251124	N/A	ANDA	ANDA219945	Umedica Laboratories USA Inc.	DICLOFENAC SODIUM	50 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (60290-083-03)
60290-083-04	60290-083	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20251124	N/A	ANDA	ANDA219945	Umedica Laboratories USA Inc.	DICLOFENAC SODIUM	50 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (60290-083-04)
60290-084-01	60290-084	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20251124	N/A	ANDA	ANDA219945	Umedica Laboratories USA Inc.	DICLOFENAC SODIUM	75 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (60290-084-01)
60290-084-02	60290-084	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20251124	N/A	ANDA	ANDA219945	Umedica Laboratories USA Inc.	DICLOFENAC SODIUM	75 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (60290-084-02)
60290-084-03	60290-084	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20251124	N/A	ANDA	ANDA219945	Umedica Laboratories USA Inc.	DICLOFENAC SODIUM	75 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (60290-084-03)
60290-084-04	60290-084	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20251124	N/A	ANDA	ANDA219945	Umedica Laboratories USA Inc.	DICLOFENAC SODIUM	75 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (60290-084-04)