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
72162-1693-5	72162-1693	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20170404	N/A	ANDA	ANDA203253	Bryant Ranch Prepack	SPIRONOLACTONE	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72162-1693-5)
72162-1694-1	72162-1694	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20170404	N/A	ANDA	ANDA203253	Bryant Ranch Prepack	SPIRONOLACTONE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72162-1694-1)
63187-861-30	63187-861	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20170601	N/A	ANDA	ANDA203253	Proficient Rx LP	SPIRONOLACTONE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-861-30)
63187-861-60	63187-861	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20170601	N/A	ANDA	ANDA203253	Proficient Rx LP	SPIRONOLACTONE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-861-60)
63187-861-90	63187-861	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20170601	N/A	ANDA	ANDA203253	Proficient Rx LP	SPIRONOLACTONE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-861-90)
42708-101-30	42708-101	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20191018	N/A	ANDA	ANDA203253	QPharma, Inc.	SPIRONOLACTONE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42708-101-30)