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
63629-1830-7	63629-1830	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20230301	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	25 mg/1	10 TABLET in 1 BOTTLE (63629-1830-7)
53489-143-01	53489-143	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	19860723	N/A	ANDA	ANDA089424	Sun Pharmaceutical Industries, Inc.	SPIRONOLACTONE	25 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (53489-143-01)
53489-143-05	53489-143	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	19860723	N/A	ANDA	ANDA089424	Sun Pharmaceutical Industries, Inc.	SPIRONOLACTONE	25 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (53489-143-05)
53489-143-10	53489-143	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	19960723	N/A	ANDA	ANDA089424	Sun Pharmaceutical Industries, Inc.	SPIRONOLACTONE	25 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (53489-143-10)
71335-2301-1	71335-2301	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20231201	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	25 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (71335-2301-1)
71335-2301-2	71335-2301	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20231201	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	25 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (71335-2301-2)
70518-3118-2	70518-3118	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20230830	N/A	ANDA	ANDA089424	REMEDYREPACK INC.	SPIRONOLACTONE	25 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (70518-3118-2)
50090-6601-0	50090-6601	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230821	N/A	ANDA	ANDA089424	A-S Medication Solutions	SPIRONOLACTONE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6601-0)