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
CEFZIL	050664	001	NDA	CEFPROZIL	TABLET;ORAL	250MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1991/12/23	1991/12/23	CORDEN PHARMA	Discontinued
CEFZIL	050664	002	NDA	CEFPROZIL	TABLET;ORAL	500MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1991/12/23	1991/12/23	CORDEN PHARMA	Discontinued
CEFZIL	050665	001	NDA	CEFPROZIL	FOR SUSPENSION;ORAL	125MG/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1991/12/23	1991/12/23	CORDEN PHARMA	Discontinued
CEFZIL	050665	002	NDA	CEFPROZIL	FOR SUSPENSION;ORAL	250MG/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1991/12/23	1991/12/23	CORDEN PHARMA	Discontinued
CEFZIL	050665	001	NDA	CEFPROZIL	FOR SUSPENSION;ORAL	125MG/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	2004/06/23	1991/12/23	CORDEN PHARMA	Discontinued
CEFZIL	050665	002	NDA	CEFPROZIL	FOR SUSPENSION;ORAL	250MG/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	2004/06/23	1991/12/23	CORDEN PHARMA	Discontinued