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
CEPHALEXIN	062779	001	ANDA	CEPHALEXIN	FOR SUSPENSION;ORAL	EQ 125MG BASE/5ML	No	No	--	1987/12/22	VITARINE	Discontinued
CEPHALEXIN	062781	001	ANDA	CEPHALEXIN	FOR SUSPENSION;ORAL	EQ 250MG BASE/5ML	No	No	--	1987/12/22	VITARINE	Discontinued
CEPHALEXIN	062809	001	ANDA	CEPHALEXIN	CAPSULE;ORAL	EQ 250MG BASE	No	No	--	1987/04/22	PUREPAC PHARM	Discontinued
CEPHALEXIN	062809	002	ANDA	CEPHALEXIN	CAPSULE;ORAL	EQ 500MG BASE	No	No	--	1987/04/22	PUREPAC PHARM	Discontinued
CEPHALEXIN	062821	001	ANDA	CEPHALEXIN	CAPSULE;ORAL	EQ 250MG BASE	No	No	--	1988/02/05	TEVA	Discontinued
CEPHALEXIN	062823	001	ANDA	CEPHALEXIN	CAPSULE;ORAL	EQ 500MG BASE	No	No	--	1988/02/05	TEVA	Discontinued
CEPHALEXIN	062863	001	ANDA	CEPHALEXIN	TABLET;ORAL	EQ 250MG BASE	No	No	--	1988/08/11	VITARINE	Discontinued
CEPHALEXIN	062863	002	ANDA	CEPHALEXIN	TABLET;ORAL	EQ 500MG BASE	No	No	--	1988/08/11	VITARINE	Discontinued
CEPHALEXIN	062863	003	ANDA	CEPHALEXIN	TABLET;ORAL	EQ 1GM BASE	No	No	--	1988/08/11	VITARINE	Discontinued
CEPHALEXIN	062867	001	ANDA	CEPHALEXIN	FOR SUSPENSION;ORAL	EQ 250MG BASE/5ML	No	No	--	1988/04/15	TEVA	Discontinued
CEPHALEXIN	062873	001	ANDA	CEPHALEXIN	FOR SUSPENSION;ORAL	EQ 125MG BASE/5ML	No	No	--	1988/05/23	TEVA	Discontinued
CEPHALEXIN	062973	001	ANDA	CEPHALEXIN	CAPSULE;ORAL	EQ 250MG BASE	No	No	--	1988/11/08	APOTHECON	Discontinued
CEPHALEXIN	062974	001	ANDA	CEPHALEXIN	CAPSULE;ORAL	EQ 500MG BASE	No	No	--	1988/11/23	APOTHECON	Discontinued
CEPHALEXIN	061969	001	ANDA	CEPHALEXIN	CAPSULE;ORAL	EQ 250MG BASE	No	No	1976/04/26	Approved Prior to Jan 1, 1982	IVAX SUB TEVA PHARMS	Discontinued
CEPHALEXIN	061969	002	ANDA	CEPHALEXIN	CAPSULE;ORAL	EQ 500MG BASE	No	No	1976/04/26	Approved Prior to Jan 1, 1982	IVAX SUB TEVA PHARMS	Discontinued
CEPHALEXIN	062117	001	ANDA	CEPHALEXIN	FOR SUSPENSION;ORAL	EQ 100MG BASE/ML *Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1978/03/27	Approved Prior to Jan 1, 1982	FACTA FARMA	Discontinued
CEPHALEXIN	062117	002	ANDA	CEPHALEXIN	FOR SUSPENSION;ORAL	EQ 125MG BASE/5ML *Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1978/03/27	Approved Prior to Jan 1, 1982	FACTA FARMA	Discontinued
CEPHALEXIN	062117	003	ANDA	CEPHALEXIN	FOR SUSPENSION;ORAL	EQ 250MG BASE/5ML *Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1978/03/27	Approved Prior to Jan 1, 1982	FACTA FARMA	Discontinued
CEPHALEXIN	062118	001	ANDA	CEPHALEXIN	CAPSULE;ORAL	EQ 250MG BASE	No	No	1978/03/27	Approved Prior to Jan 1, 1982	FACTA FARMA	Discontinued
CEPHALEXIN	062118	002	ANDA	CEPHALEXIN	CAPSULE;ORAL	EQ 500MG BASE	No	No	1978/03/27	Approved Prior to Jan 1, 1982	FACTA FARMA	Discontinued