美国FDA药品数据库-药物在线

商品名	申请号	产品号	申请类型	活性成分	剂型/给药途径	规格/剂量	RLD	RS	申请号原始批准/暂定批准日期	产品号批准日期	申请人	市场状态
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE	088025	001	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	--	1984/11/23	ASCOT	Discontinued
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE	086513	001	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	1979/08/03	Approved Prior to Jan 1, 1982	MYLAN	Prescription
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE	086881	001	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	1980/07/10	Approved Prior to Jan 1, 1982	CHARTWELL RX	Discontinued
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE	087267	001	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	1981/04/16	Approved Prior to Jan 1, 1982	MUTUAL PHARM	Discontinued
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE	087398	001	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	1981/11/24	Approved Prior to Jan 1, 1982	WATSON LABS	Discontinued
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE	089137	001	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	1985/08/26	1985/08/26	SUPERPHARM	Discontinued
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE	087999	001	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	1985/11/06	1985/11/06	PUREPAC PHARM	Discontinued
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE	089534	001	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	1987/07/02	1987/07/02	SUN PHARM INDUSTRIES	Prescription