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
72162-1627-2	72162-1627	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230516	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72162-1627-2)
72162-1627-3	72162-1627	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230516	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72162-1627-3)
72162-1627-4	72162-1627	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230516	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72162-1627-4)
72162-1627-5	72162-1627	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230516	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72162-1627-5)
72162-1627-7	72162-1627	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230516	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72162-1627-7)