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
63629-4094-4	63629-4094	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20220217	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63629-4094-4)
63629-1062-1	63629-1062	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	19860723	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	25 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (63629-1062-1)
63629-1067-1	63629-1067	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20200921	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-1067-1)
63629-1067-2	63629-1067	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20201201	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-1067-2)
63629-1067-3	63629-1067	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20201214	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-1067-3)
63629-1067-4	63629-1067	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20221026	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-1067-4)
71335-2203-1	71335-2203	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230804	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2203-1)
63629-1093-1	63629-1093	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	19860723	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-1093-1)
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)
63629-1061-1	63629-1061	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	19860723	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	25 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (63629-1061-1)
63629-1066-1	63629-1066	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	19860723	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-1066-1)
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)
71335-2207-1	71335-2207	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230804	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2207-1)
63629-1092-1	63629-1092	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	19860723	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-1092-1)
53489-329-01	53489-329	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	19860723	N/A	ANDA	ANDA089424	Sun Pharmaceutical Industries, Inc.	SPIRONOLACTONE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-01)
53489-329-02	53489-329	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	19860723	N/A	ANDA	ANDA089424	Sun Pharmaceutical Industries, Inc.	SPIRONOLACTONE	100 mg/1	50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-02)
53489-329-03	53489-329	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	19860723	N/A	ANDA	ANDA089424	Sun Pharmaceutical Industries, Inc.	SPIRONOLACTONE	100 mg/1	250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-03)