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
50742-279-01	50742-279	HUMAN PRESCRIPTION DRUG	Diclofenac Potassium	diclofenac potassium	TABLET, FILM COATED	ORAL	20211011	N/A	ANDA	ANDA215585	Ingenus Pharmaceuticals, LLC	DICLOFENAC POTASSIUM	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50742-279-01)
70518-3538-0	70518-3538	HUMAN PRESCRIPTION DRUG	Diclofenac Potassium	diclofenac potassium	TABLET, FILM COATED	ORAL	20220926	N/A	ANDA	ANDA215585	REMEDYREPACK INC.	DICLOFENAC POTASSIUM	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3538-0)
70518-3538-1	70518-3538	HUMAN PRESCRIPTION DRUG	Diclofenac Potassium	diclofenac potassium	TABLET, FILM COATED	ORAL	20221219	N/A	ANDA	ANDA215585	REMEDYREPACK INC.	DICLOFENAC POTASSIUM	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3538-1)
70518-3538-2	70518-3538	HUMAN PRESCRIPTION DRUG	Diclofenac Potassium	diclofenac potassium	TABLET, FILM COATED	ORAL	20230207	N/A	ANDA	ANDA215585	REMEDYREPACK INC.	DICLOFENAC POTASSIUM	50 mg/1	270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3538-2)
70518-3538-3	70518-3538	HUMAN PRESCRIPTION DRUG	Diclofenac Potassium	diclofenac potassium	TABLET, FILM COATED	ORAL	20230406	N/A	ANDA	ANDA215585	REMEDYREPACK INC.	DICLOFENAC POTASSIUM	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3538-3)
68071-2892-3	68071-2892	HUMAN PRESCRIPTION DRUG	Diclofenac Potassium	diclofenac potassium	TABLET, FILM COATED	ORAL	20221201	N/A	ANDA	ANDA215585	NuCare Pharmaceuticals,Inc.	DICLOFENAC POTASSIUM	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2892-3)