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
CEFTIN	050605	001	NDA	CEFUROXIME AXETIL	TABLET;ORAL	EQ 125MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1987/12/28	1987/12/28	GLAXOSMITHKLINE	Discontinued
CEFTIN	050605	002	NDA	CEFUROXIME AXETIL	TABLET;ORAL	EQ 250MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1987/12/28	1987/12/28	GLAXOSMITHKLINE	Discontinued
CEFTIN	050605	003	NDA	CEFUROXIME AXETIL	TABLET;ORAL	EQ 500MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1987/12/28	1987/12/28	GLAXOSMITHKLINE	Discontinued
CEFTIN	050672	001	NDA	CEFUROXIME AXETIL	FOR SUSPENSION;ORAL	EQ 125MG BASE/5ML	Yes	No	1994/06/30	1994/06/30	GLAXOSMITHKLINE	Discontinued
CEFTIN	050672	002	NDA	CEFUROXIME AXETIL	FOR SUSPENSION;ORAL	EQ 250MG BASE/5ML	Yes	No	1994/06/30	1997/04/29	GLAXOSMITHKLINE	Discontinued