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 W/ RESERPINE	086331	001	ANDA	HYDROCHLOROTHIAZIDE; RESERPINE	TABLET;ORAL	50MG;0.125MG	No	No	1978/06/12	Approved Prior to Jan 1, 1982	WATSON LABS	Discontinued
HYDROCHLOROTHIAZIDE	085004	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	25MG	No	No	1978/07/13	Approved Prior to Jan 1, 1982	ROXANE	Discontinued
HYDROCHLOROTHIAZIDE	085005	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG	No	No	1978/07/13	Approved Prior to Jan 1, 1982	ROXANE	Discontinued
HYDROCHLOROTHIAZIDE	086087	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG	No	No	1978/07/17	Approved Prior to Jan 1, 1982	WATSON LABS	Discontinued
HYDROCHLOROTHIAZIDE	086594	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG	No	No	1978/10/05	Approved Prior to Jan 1, 1982	WATSON LABS	Discontinued
HYDROCHLOROTHIAZIDE	086597	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG	No	No	1978/10/11	Approved Prior to Jan 1, 1982	PVT FORM	Discontinued
HYDROCHLOROTHIAZIDE	085219	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG	No	No	1979/03/12	Approved Prior to Jan 1, 1982	AUROLIFE PHARMA LLC	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 W/ HYDROCHLOROTHIAZIDE	087004	002	ANDA	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	TABLET;ORAL	25MG;25MG	No	No	1980/05/07	1982/05/24	IVAX PHARMS	Discontinued
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
HYDROCHLOROTHIAZIDE	087059	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	25MG	No	No	1980/11/05	Approved Prior to Jan 1, 1982	OXFORD PHARMS	Prescription
HYDROCHLOROTHIAZIDE	087060	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	100MG	No	No	1980/11/05	Approved Prior to Jan 1, 1982	DAVA PHARMS INC	Discontinued
HYDROCHLOROTHIAZIDE	087068	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG	No	No	1980/11/05	Approved Prior to Jan 1, 1982	OXFORD PHARMS	Prescription
HYDROCHLOROTHIAZIDE	087002	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	100MG	No	No	1981/02/09	Approved Prior to Jan 1, 1982	WATSON LABS	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
RESERPINE, HYDRALAZINE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE	087556	001	ANDA	HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE; RESERPINE	TABLET;ORAL	25MG;15MG;0.1MG	No	No	1981/08/06	Approved Prior to Jan 1, 1982	WATSON LABS	Discontinued
HYDROCHLOROTHIAZIDE	085054	002	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	25MG	No	No	1981/08/20	Approved Prior to Jan 1, 1982	ACTAVIS ELIZABETH	Discontinued
HYDROCHLOROTHIAZIDE	085208	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG	No	No	1981/08/20	Approved Prior to Jan 1, 1982	ACTAVIS ELIZABETH	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
HYDROCHLOROTHIAZIDE	087610	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG	No	No	1981/12/07	Approved Prior to Jan 1, 1982	VANGARD	Discontinued