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
68071-3375-3	68071-3375	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20170711	N/A	ANDA	ANDA203512	NuCare Pharmaceuticals, Inc.	SPIRONOLACTONE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-3375-3)
68071-3375-6	68071-3375	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20170711	N/A	ANDA	ANDA203512	NuCare Pharmaceuticals, Inc.	SPIRONOLACTONE	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68071-3375-6)
68071-3375-8	68071-3375	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20170711	N/A	ANDA	ANDA203512	NuCare Pharmaceuticals, Inc.	SPIRONOLACTONE	25 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (68071-3375-8)
68071-3375-9	68071-3375	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20170711	N/A	ANDA	ANDA203512	NuCare Pharmaceuticals, Inc.	SPIRONOLACTONE	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-3375-9)