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
63629-1063-1	63629-1063	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20200605	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	25 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (63629-1063-1)
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)
53489-328-01	53489-328	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	19860723	N/A	ANDA	ANDA089424	Sun Pharmaceutical Industries, Inc.	SPIRONOLACTONE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-01)
53489-328-02	53489-328	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	19860723	N/A	ANDA	ANDA089424	Sun Pharmaceutical Industries, Inc.	SPIRONOLACTONE	50 mg/1	50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-02)
53489-328-03	53489-328	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	19860723	N/A	ANDA	ANDA089424	Sun Pharmaceutical Industries, Inc.	SPIRONOLACTONE	50 mg/1	250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-03)
53489-328-05	53489-328	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	19860723	N/A	ANDA	ANDA089424	Sun Pharmaceutical Industries, Inc.	SPIRONOLACTONE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-05)
53489-328-06	53489-328	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	19860723	N/A	ANDA	ANDA089424	Sun Pharmaceutical Industries, Inc.	SPIRONOLACTONE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-06)
63629-1064-1	63629-1064	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20200915	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (63629-1064-1)
63629-1064-2	63629-1064	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20200921	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	25 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (63629-1064-2)
63629-1064-3	63629-1064	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20200921	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (63629-1064-3)
63629-1064-4	63629-1064	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20230516	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	25 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (63629-1064-4)
50090-0136-0	50090-0136	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20141128	N/A	ANDA	ANDA089424	A-S Medication Solutions	SPIRONOLACTONE	25 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (50090-0136-0)
50090-0136-1	50090-0136	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20141128	N/A	ANDA	ANDA089424	A-S Medication Solutions	SPIRONOLACTONE	25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (50090-0136-1)
50090-0136-6	50090-0136	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20141128	N/A	ANDA	ANDA089424	A-S Medication Solutions	SPIRONOLACTONE	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (50090-0136-6)
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)