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)
63629-1064-1	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)
63629-1065-1	63629-1065	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	19860723	N/A	ANDA	ANDA089424	Bryant Ranch Prepack	SPIRONOLACTONE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-1065-1)
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)
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)
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)
63629-1061-1	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)
63629-1093-1	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)
76420-556-01	76420-556	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20230407	N/A	ANDA	ANDA089424	Asclemed USA, Inc.	SPIRONOLACTONE	25 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (76420-556-01)
76420-556-30	76420-556	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20230407	N/A	ANDA	ANDA089424	Asclemed USA, Inc.	SPIRONOLACTONE	25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (76420-556-30)
76420-556-60	76420-556	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20230407	N/A	ANDA	ANDA089424	Asclemed USA, Inc.	SPIRONOLACTONE	25 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (76420-556-60)
76420-556-90	76420-556	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET	ORAL	20230407	N/A	ANDA	ANDA089424	Asclemed USA, Inc.	SPIRONOLACTONE	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (76420-556-90)
76420-557-01	76420-557	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230407	N/A	ANDA	ANDA089424	Asclemed USA, Inc.	SPIRONOLACTONE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-557-01)
76420-557-30	76420-557	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230407	N/A	ANDA	ANDA089424	Asclemed USA, Inc.	SPIRONOLACTONE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-557-30)