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 W/ HYDROCHLOROTHIAZIDE	085974	001	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	--	Approved Prior to Jan 1, 1982	WATSON LABS	Discontinued
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE	086026	001	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	--	Approved Prior to Jan 1, 1982	WATSON LABS	Discontinued
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE	087511	001	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	--	Approved Prior to Jan 1, 1982	LEDERLE	Discontinued
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE	087553	001	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	--	Approved Prior to Jan 1, 1982	UPSHER SMITH	Discontinued
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE	087651	001	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	--	Approved Prior to Jan 1, 1982	USL PHARMA	Discontinued
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE	087948	001	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	--	1983/02/22	PARKE DAVIS	Discontinued
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE	088054	001	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	--	1983/08/18	PUREPAC PHARM	Discontinued
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE	087004	002	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	1980/05/07	1982/05/24	IVAX PHARMS	Discontinued
SPIRONOLACTONE W/ HYDROCHLOROTHIAZIDE	087655	001	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	1981/12/14	Approved Prior to Jan 1, 1982	VANGARD	Discontinued