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	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
HYDRALAZINE HYDROCHLORIDE, HYDROCHLOROTHIAZIDE AND RESERPINE	084291	001	ANDA	HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE; RESERPINE	TABLET;ORAL	25MG;15MG;0.1MG	No	No	1975/02/03	Approved Prior to Jan 1, 1982	IVAX SUB TEVA PHARMS	Discontinued
RESERPINE AND HYDROCHLOROTHIAZIDE	084580	001	ANDA	HYDROCHLOROTHIAZIDE; RESERPINE	TABLET;ORAL	25MG;0.125MG	No	No	1975/05/30	Approved Prior to Jan 1, 1982	BARR	Discontinued
HYDROCHLOROTHIAZIDE	084658	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG	No	No	1975/09/24	Approved Prior to Jan 1, 1982	IVAX SUB TEVA PHARMS	Discontinued
RESERPINE AND HYDROCHLOROTHIAZIDE	084579	001	ANDA	HYDROCHLOROTHIAZIDE; RESERPINE	TABLET;ORAL	50MG;0.125MG	No	No	1975/09/30	Approved Prior to Jan 1, 1982	BARR	Discontinued
HYDROCHLOROTHIAZIDE	084324	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG	No	No	1976/06/24	Approved Prior to Jan 1, 1982	LANNETT CO INC	Discontinued
HYDROCHLOROTHIAZIDE	084325	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	25MG	No	No	1976/06/24	Approved Prior to Jan 1, 1982	LANNETT CO INC	Discontinued
HYDROCHLOROTHIAZIDE	084776	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	25MG	No	No	1976/09/21	Approved Prior to Jan 1, 1982	INWOOD LABS	Discontinued
HYDROCHLOROTHIAZIDE	084776	002	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG	No	No	1976/09/21	Approved Prior to Jan 1, 1982	INWOOD LABS	Discontinued
HYDROCHLOROTHIAZIDE	084912	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG	No	No	1976/12/17	Approved Prior to Jan 1, 1982	CHARTWELL RX	Discontinued
HYDROCHLOROTHIAZIDE W/ RESERPINE	084466	001	ANDA	HYDROCHLOROTHIAZIDE; RESERPINE	TABLET;ORAL	25MG;0.125MG	No	No	1977/01/07	Approved Prior to Jan 1, 1982	WATSON LABS	Discontinued
HYDROCHLOROTHIAZIDE W/ RESERPINE	084467	001	ANDA	HYDROCHLOROTHIAZIDE; RESERPINE	TABLET;ORAL	50MG;0.125MG	No	No	1977/01/07	Approved Prior to Jan 1, 1982	WATSON LABS	Discontinued
HYDROCHLOROTHIAZIDE	084878	001	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG	No	No	1977/01/31	Approved Prior to Jan 1, 1982	HIKMA INTL PHARMS	Discontinued
HYDROCHLOROTHIAZIDE	084878	002	ANDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	25MG	No	No	1977/01/31	2006/07/12	HIKMA INTL PHARMS	Discontinued