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
DIURIL	011145	002	NDA	CHLOROTHIAZIDE	TABLET;ORAL	500MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1958/09/04	Approved Prior to Jan 1, 1982	RISING	Discontinued
DIURIL	011145	004	NDA	CHLOROTHIAZIDE	TABLET;ORAL	250MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1958/09/04	Approved Prior to Jan 1, 1982	RISING	Discontinued
DIURIL	011145	005	NDA	CHLOROTHIAZIDE SODIUM	INJECTABLE;INJECTION	EQ 500MG BASE/VIAL	Yes	No	1958/09/04	Approved Prior to Jan 1, 1982	RISING	Discontinued
HYDRODIURIL	011835	003	NDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	25MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1959/02/24	Approved Prior to Jan 1, 1982	MERCK	Discontinued
HYDRODIURIL	011835	006	NDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1959/02/24	Approved Prior to Jan 1, 1982	MERCK	Discontinued
HYDRODIURIL	011835	007	NDA	HYDROCHLOROTHIAZIDE	TABLET;ORAL	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1959/02/24	Approved Prior to Jan 1, 1982	MERCK	Discontinued
DIURIL	011870	001	NDA	CHLOROTHIAZIDE	SUSPENSION;ORAL	250MG/5ML	Yes	Yes	1961/10/06	Approved Prior to Jan 1, 1982	SALIX PHARMS	Prescription