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
60290-061-01	60290-061	HUMAN PRESCRIPTION DRUG	DICLOFENAC POTASSIUM	Diclofenac potassium	POWDER, FOR SOLUTION	ORAL	20260215	N/A	ANDA	ANDA217010	Umedica Laboratories USA Inc.	DICLOFENAC POTASSIUM	50 mg/1	1 POWDER, FOR SOLUTION in 1 PACKET (60290-061-01)
60290-061-02	60290-061	HUMAN PRESCRIPTION DRUG	DICLOFENAC POTASSIUM	Diclofenac potassium	POWDER, FOR SOLUTION	ORAL	20260215	N/A	ANDA	ANDA217010	Umedica Laboratories USA Inc.	DICLOFENAC POTASSIUM	50 mg/1	9 POWDER, FOR SOLUTION in 1 CARTON (60290-061-02)
75834-338-01	75834-338	HUMAN PRESCRIPTION DRUG	DICLOFENAC POTASSIUM	Diclofenac potassium	POWDER, FOR SOLUTION	ORAL	20251215	N/A	ANDA	ANDA217010	Nivagen Pharmaceuticals, Inc.	DICLOFENAC POTASSIUM	50 mg/1	1 POWDER, FOR SOLUTION in 1 PACKET (75834-338-01)
75834-338-02	75834-338	HUMAN PRESCRIPTION DRUG	DICLOFENAC POTASSIUM	Diclofenac potassium	POWDER, FOR SOLUTION	ORAL	20251215	N/A	ANDA	ANDA217010	Nivagen Pharmaceuticals, Inc.	DICLOFENAC POTASSIUM	50 mg/1	9 POWDER, FOR SOLUTION in 1 CARTON (75834-338-02)