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
KYTRIL	020239	001	NDA	GRANISETRON HYDROCHLORIDE	INJECTABLE;INJECTION	EQ 3MG BASE/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1993/12/29	1993/12/29	ROCHE	Discontinued
KYTRIL	020239	002	NDA	GRANISETRON HYDROCHLORIDE	INJECTABLE;INJECTION	EQ 4MG BASE/4ML (EQ 1MG BASE/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1993/12/29	1994/03/11	ROCHE	Discontinued
KYTRIL	020239	003	NDA	GRANISETRON HYDROCHLORIDE	INJECTABLE;INJECTION	EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1993/12/29	2004/09/17	ROCHE	Discontinued
KYTRIL	020239	004	NDA	GRANISETRON HYDROCHLORIDE	INJECTABLE;INJECTION	EQ 1MG BASE/ML (EQ 1MG BASE/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1993/12/29	1994/03/11	ROCHE	Discontinued
KYTRIL	020305	001	NDA	GRANISETRON HYDROCHLORIDE	TABLET;ORAL	EQ 1MG BASE Federal Register determination that product was not withdrawn or discontinued for safety or effectiveness reasons	Yes	No	1995/03/16	1995/03/16	ROCHE	Discontinued
KYTRIL	020305	002	NDA	GRANISETRON HYDROCHLORIDE	TABLET;ORAL	EQ 2MG BASE Federal Register determination that product was not withdrawn or discontinued for safety or effectiveness reasons	Yes	No	1995/03/16	1998/06/15	ROCHE	Discontinued
KYTRIL	021238	001	NDA	GRANISETRON HYDROCHLORIDE	SOLUTION;ORAL	EQ 2MG BASE/10ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	2001/06/27	2001/06/27	ROCHE	Discontinued