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
STELAZINE	011552	001	NDA	TRIFLUOPERAZINE HYDROCHLORIDE	TABLET;ORAL	EQ 1MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1959/04/16	Approved Prior to Jan 1, 1982	GLAXOSMITHKLINE	Discontinued
STELAZINE	011552	002	NDA	TRIFLUOPERAZINE HYDROCHLORIDE	TABLET;ORAL	EQ 2MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1959/04/16	Approved Prior to Jan 1, 1982	GLAXOSMITHKLINE	Discontinued
STELAZINE	011552	003	NDA	TRIFLUOPERAZINE HYDROCHLORIDE	TABLET;ORAL	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1959/04/16	Approved Prior to Jan 1, 1982	GLAXOSMITHKLINE	Discontinued
STELAZINE	011552	004	NDA	TRIFLUOPERAZINE HYDROCHLORIDE	TABLET;ORAL	EQ 10MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1959/04/16	Approved Prior to Jan 1, 1982	GLAXOSMITHKLINE	Discontinued
STELAZINE	011552	005	NDA	TRIFLUOPERAZINE HYDROCHLORIDE	INJECTABLE;INJECTION	EQ 2MG BASE/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1959/04/16	Approved Prior to Jan 1, 1982	GLAXOSMITHKLINE	Discontinued
STELAZINE	011552	006	NDA	TRIFLUOPERAZINE HYDROCHLORIDE	CONCENTRATE;ORAL	EQ 10MG BASE/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1959/04/16	Approved Prior to Jan 1, 1982	GLAXOSMITHKLINE	Discontinued