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
69584-854-90	69584-854	HUMAN PRESCRIPTION DRUG	Spironolactone	Spironolactone	TABLET, COATED	ORAL	20240401	N/A	ANDA	ANDA040750	Oxford Pharmaceuticals, LLC	SPIRONOLACTONE	100 mg/1	1000 TABLET, COATED in 1 BOTTLE (69584-854-90)
50090-6369-0	50090-6369	HUMAN PRESCRIPTION DRUG	Spironolactone	Spironolactone	TABLET, COATED	ORAL	20230210	N/A	ANDA	ANDA040750	A-S Medication Solutions	SPIRONOLACTONE	25 mg/1	100 TABLET, COATED in 1 BOTTLE (50090-6369-0)
50090-6369-1	50090-6369	HUMAN PRESCRIPTION DRUG	Spironolactone	Spironolactone	TABLET, COATED	ORAL	20230216	N/A	ANDA	ANDA040750	A-S Medication Solutions	SPIRONOLACTONE	25 mg/1	30 TABLET, COATED in 1 BOTTLE (50090-6369-1)
50090-6369-6	50090-6369	HUMAN PRESCRIPTION DRUG	Spironolactone	Spironolactone	TABLET, COATED	ORAL	20230216	N/A	ANDA	ANDA040750	A-S Medication Solutions	SPIRONOLACTONE	25 mg/1	90 TABLET, COATED in 1 BOTTLE (50090-6369-6)