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
DURICEF	050512	001	NDA	CEFADROXIL/CEFADROXIL HEMIHYDRATE	CAPSULE;ORAL	EQ 500MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1978/02/17	Approved Prior to Jan 1, 1982	WARNER CHILCOTT	Discontinued
DURICEF	050512	002	NDA	CEFADROXIL/CEFADROXIL HEMIHYDRATE	CAPSULE;ORAL	EQ 250MG BASE	No	No	1978/02/17	Approved Prior to Jan 1, 1982	WARNER CHILCOTT	Discontinued
DURICEF	050528	001	NDA	CEFADROXIL/CEFADROXIL HEMIHYDRATE	TABLET;ORAL	EQ 1GM BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1980/08/06	Approved Prior to Jan 1, 1982	WARNER CHILCOTT	Discontinued
DURICEF	050527	001	NDA	CEFADROXIL/CEFADROXIL HEMIHYDRATE	FOR SUSPENSION;ORAL	EQ 500MG BASE/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1980/09/12	Approved Prior to Jan 1, 1982	WARNER CHILCOTT	Discontinued
DURICEF	050527	002	NDA	CEFADROXIL/CEFADROXIL HEMIHYDRATE	FOR SUSPENSION;ORAL	EQ 125MG BASE/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1980/09/12	Approved Prior to Jan 1, 1982	WARNER CHILCOTT	Discontinued
DURICEF	050527	003	NDA	CEFADROXIL/CEFADROXIL HEMIHYDRATE	FOR SUSPENSION;ORAL	EQ 250MG BASE/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1980/09/12	Approved Prior to Jan 1, 1982	WARNER CHILCOTT	Discontinued