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
E.E.S.	050207	001	NDA	ERYTHROMYCIN ETHYLSUCCINATE	GRANULE;ORAL	EQ 200MG BASE/5ML	Yes	No	1965/04/02	Approved Prior to Jan 1, 1982	AZURITY	Prescription
E.E.S.	050297	002	NDA	ERYTHROMYCIN ETHYLSUCCINATE	TABLET, CHEWABLE;ORAL	EQ 200MG BASE	No	No	1970/08/06	Approved Prior to Jan 1, 1982	AZURITY	Discontinued
E.E.S. 200	061639	001	ANDA	ERYTHROMYCIN ETHYLSUCCINATE	SUSPENSION;ORAL	EQ 200MG BASE/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1973/10/15	Approved Prior to Jan 1, 1982	ARBOR PHARMS LLC	Discontinued
E.E.S. 400	061639	002	ANDA	ERYTHROMYCIN ETHYLSUCCINATE	SUSPENSION;ORAL	EQ 400MG BASE/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1973/10/15	Approved Prior to Jan 1, 1982	ARBOR PHARMS LLC	Discontinued
E.E.S. 400	061905	001	ANDA	ERYTHROMYCIN ETHYLSUCCINATE	TABLET;ORAL	EQ 400MG BASE	No	No	1982/08/12	Approved Prior to Jan 1, 1982	AZURITY	Discontinued
E.E.S. 400	061905	002	ANDA	ERYTHROMYCIN ETHYLSUCCINATE	TABLET;ORAL	EQ 400MG BASE	No	Yes	1982/08/12	1982/08/12	AZURITY	Prescription