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
HYDROCHLOROTHIAZIDE	089661	001	ANDA	HYDROCHLOROTHIAZIDE	SOLUTION;ORAL	50MG/5ML	No	No	--	1988/06/20	MORTON GROVE	Discontinued
ALDACTAZIDE	012616	004	NDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	Yes	No	1961/01/27	1982/12/30	PFIZER	Prescription
ALDACTAZIDE	012616	005	NDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	50MG;50MG	Yes	No	1961/01/27	1982/12/30	PFIZER	Discontinued
DYAZIDE	016042	002	NDA	HYDROCHLOROTHIAZIDE; TRIAMTERENE	CAPSULE;ORAL	25MG;50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1965/12/02	Approved Prior to Jan 1, 1982	GLAXOSMITHKLINE LLC	Discontinued
DYAZIDE	016042	003	NDA	HYDROCHLOROTHIAZIDE; TRIAMTERENE	CAPSULE;ORAL	25MG;37.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1965/12/02	1994/03/03	GLAXOSMITHKLINE LLC	Discontinued
STANOZIDE	080126	001	ANDA	ISONIAZID	TABLET;ORAL	100MG	No	No	1972/01/21	Approved Prior to Jan 1, 1982	EVERYLIFE	Discontinued
STANOZIDE	080126	002	ANDA	ISONIAZID	TABLET;ORAL	300MG	No	No	1972/01/21	Approved Prior to Jan 1, 1982	EVERYLIFE	Discontinued
HYDROCHLOROTHIAZIDE	083177	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	25MG	Yes	No	1973/01/12	Approved Prior to Jan 1, 1982	IVAX SUB TEVA PHARMS	Prescription
HYDROCHLOROTHIAZIDE	083177	002	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG	Yes	Yes	1973/01/12	Approved Prior to Jan 1, 1982	IVAX SUB TEVA PHARMS	Prescription
HYDROCHLOROTHIAZIDE	083177	003	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	12.5MG	Yes	No	1973/01/12	2024/09/19	IVAX SUB TEVA PHARMS	Prescription
HYDROCHLOROTHIAZIDE W/ RESERPINE	083571	001	ANDA	HYDROCHLOROTHIAZIDE; RESERPINE	TABLET;ORAL	25MG;0.125MG	No	No	1973/11/20	Approved Prior to Jan 1, 1982	IVAX SUB TEVA PHARMS	Discontinued
HYDROCHLOROTHIAZIDE W/ RESERPINE	083572	001	ANDA	HYDROCHLOROTHIAZIDE; RESERPINE	TABLET;ORAL	25MG;0.1MG	No	No	1973/11/26	Approved Prior to Jan 1, 1982	IVAX SUB TEVA PHARMS	Discontinued
HYDROCHLOROTHIAZIDE W/ RESERPINE	083568	001	ANDA	HYDROCHLOROTHIAZIDE; RESERPINE	TABLET;ORAL	50MG;0.1MG	No	No	1973/12/04	Approved Prior to Jan 1, 1982	IVAX SUB TEVA PHARMS	Discontinued
HYDROCHLOROTHIAZIDE W/ RESERPINE	083573	001	ANDA	HYDROCHLOROTHIAZIDE; RESERPINE	TABLET;ORAL	50MG;0.125MG	No	No	1973/12/11	Approved Prior to Jan 1, 1982	IVAX SUB TEVA PHARMS	Discontinued
HYDROCHLOROTHIAZIDE	083809	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG	No	No	1974/07/02	Approved Prior to Jan 1, 1982	WHITEWORTH TOWN PLSN	Discontinued
HYDROCHLOROTHIAZIDE	083809	002	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	25MG	No	No	1974/07/02	Approved Prior to Jan 1, 1982	WHITEWORTH TOWN PLSN	Discontinued
HYDROCHLOROTHIAZIDE	083972	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	25MG	No	No	1974/10/03	Approved Prior to Jan 1, 1982	SUN PHARM INDUSTRIES	Discontinued
HYDROCHLOROTHIAZIDE	083972	002	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG	No	No	1974/10/03	Approved Prior to Jan 1, 1982	SUN PHARM INDUSTRIES	Discontinued
HYDROCHLOROTHIAZIDE	083972	003	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	100MG	No	No	1974/10/03	Approved Prior to Jan 1, 1982	SUN PHARM INDUSTRIES	Discontinued
HYDROCHLOROTHIAZIDE	083232	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG	No	No	1975/01/24	Approved Prior to Jan 1, 1982	WATSON LABS TEVA	Discontinued