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
63629-4094-5	63629-4094	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20211006	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63629-4094-5)
53489-329-10	53489-329	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	19860723	N/A	ANDA	ANDA089424	Sun Pharmaceutical Industries, Inc.	SPIRONOLACTONE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-10)
50090-6432-0	50090-6432	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230411	N/A	ANDA	ANDA089424	A-S Medication Solutions	SPIRONOLACTONE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6432-0)
50090-6432-1	50090-6432	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230411	N/A	ANDA	ANDA089424	A-S Medication Solutions	SPIRONOLACTONE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-6432-1)