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
CECLOR	050521	001	NDA	CEFACLOR	CAPSULE;ORAL	EQ 250MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1979/04/04	Approved Prior to Jan 1, 1982	LILLY	Discontinued
CECLOR	050521	002	NDA	CEFACLOR	CAPSULE;ORAL	EQ 500MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1979/04/04	Approved Prior to Jan 1, 1982	LILLY	Discontinued
CECLOR	050522	001	NDA	CEFACLOR	FOR SUSPENSION;ORAL	EQ 125MG BASE/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1979/04/04	Approved Prior to Jan 1, 1982	LILLY	Discontinued
CECLOR	050522	002	NDA	CEFACLOR	FOR SUSPENSION;ORAL	EQ 250MG BASE/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1979/04/04	Approved Prior to Jan 1, 1982	LILLY	Discontinued
CECLOR CD	050673	001	NDA	CEFACLOR	TABLET, EXTENDED RELEASE;ORAL	EQ 375MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1996/06/28	1996/06/28	LILLY	Discontinued
CECLOR CD	050673	002	NDA	CEFACLOR	TABLET, EXTENDED RELEASE;ORAL	EQ 500MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1996/06/28	1996/06/28	LILLY	Discontinued