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
16729-225-17	16729-225	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20170615	N/A	ANDA	ANDA203512	Accord Healthcare, Inc.	SPIRONOLACTONE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16729-225-17)
71610-288-30	71610-288	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20190531	N/A	ANDA	ANDA203512	Aphena Pharma Solutions - Tennessee, LLC	SPIRONOLACTONE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71610-288-30)
71610-288-45	71610-288	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20190531	N/A	ANDA	ANDA203512	Aphena Pharma Solutions - Tennessee, LLC	SPIRONOLACTONE	100 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71610-288-45)
71610-288-60	71610-288	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20190531	N/A	ANDA	ANDA203512	Aphena Pharma Solutions - Tennessee, LLC	SPIRONOLACTONE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71610-288-60)