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
71610-970-45	71610-970	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20251203	N/A	ANDA	ANDA089424	Aphena Pharma Solutions - Tennessee, LLC	SPIRONOLACTONE	25 mg/1	45 TABLET in 1 BOTTLE (71610-970-45)
71610-970-60	71610-970	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20251203	N/A	ANDA	ANDA089424	Aphena Pharma Solutions - Tennessee, LLC	SPIRONOLACTONE	25 mg/1	90 TABLET in 1 BOTTLE (71610-970-60)
50090-6408-0	50090-6408	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230323	N/A	ANDA	ANDA089424	A-S Medication Solutions	SPIRONOLACTONE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (50090-6408-0)
50090-6408-1	50090-6408	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230323	N/A	ANDA	ANDA089424	A-S Medication Solutions	SPIRONOLACTONE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6408-1)
50090-6408-2	50090-6408	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230323	N/A	ANDA	ANDA089424	A-S Medication Solutions	SPIRONOLACTONE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-6408-2)