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
DURANEST	017751	003	NDA	ETIDOCAINE HYDROCHLORIDE	INJECTABLE;INJECTION	0.5% Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1976/08/30	Approved Prior to Jan 1, 1982	ASTRAZENECA	Discontinued
DURANEST	017751	004	NDA	EPINEPHRINE; ETIDOCAINE HYDROCHLORIDE	INJECTABLE;INJECTION	0.005MG/ML;0.5% Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1976/08/30	Approved Prior to Jan 1, 1982	ASTRAZENECA	Discontinued
DURANEST	017751	005	NDA	ETIDOCAINE HYDROCHLORIDE	INJECTABLE;INJECTION	1% Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1976/08/30	Approved Prior to Jan 1, 1982	ASTRAZENECA	Discontinued
DURANEST	017751	006	NDA	EPINEPHRINE BITARTRATE; ETIDOCAINE HYDROCHLORIDE	INJECTABLE;INJECTION	0.005MG/ML;1% Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1976/08/30	Approved Prior to Jan 1, 1982	ASTRAZENECA	Discontinued
DURANEST	017751	007	NDA	EPINEPHRINE BITARTRATE; ETIDOCAINE HYDROCHLORIDE	INJECTABLE;INJECTION	0.005MG/ML;1.5% Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1976/08/30	Approved Prior to Jan 1, 1982	ASTRAZENECA	Discontinued
DURANEST	021384	001	NDA	EPINEPHRINE BITARTRATE; ETIDOCAINE HYDROCHLORIDE	INJECTABLE;INJECTION	0.005MG/ML;1.5% Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1976/08/30	Approved Prior to Jan 1, 1982	DENTSPLY PHARM	Discontinued