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
ATOMOXETINE HYDROCHLORIDE	079017	001	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE;ORAL	EQ 18MG BASE	No	No	2010/09/16	2010/09/16	ZYDUS PHARMS USA INC	Prescription
ATOMOXETINE HYDROCHLORIDE	079017	002	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE;ORAL	EQ 25MG BASE	No	No	2010/09/16	2010/09/16	ZYDUS PHARMS USA INC	Prescription
ATOMOXETINE HYDROCHLORIDE	079017	003	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE;ORAL	EQ 40MG BASE	No	No	2010/09/16	2010/09/16	ZYDUS PHARMS USA INC	Prescription
ATOMOXETINE HYDROCHLORIDE	079017	004	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE;ORAL	EQ 60MG BASE	No	No	2010/09/16	2010/09/16	ZYDUS PHARMS USA INC	Prescription
ATOMOXETINE HYDROCHLORIDE	079017	005	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE;ORAL	EQ 80MG BASE	No	No	2010/09/16	2010/09/16	ZYDUS PHARMS USA INC	Prescription
ATOMOXETINE HYDROCHLORIDE	079017	006	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE;ORAL	EQ 100MG BASE	No	No	2010/09/16	2010/09/16	ZYDUS PHARMS USA INC	Prescription
ATOMOXETINE HYDROCHLORIDE	079017	007	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE;ORAL	EQ 10MG BASE	No	No	2010/09/16	2023/04/05	ZYDUS PHARMS USA INC	Prescription
ATOMOXETINE HYDROCHLORIDE	078940	002	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE;ORAL	18MG	No	No	2012/05/11 (TA)	--	ACTAVIS ELIZABETH	None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE	078940	003	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE;ORAL	25MG	No	No	2012/05/11 (TA)	--	ACTAVIS ELIZABETH	None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE	078940	004	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE;ORAL	40MG	No	No	2012/05/11 (TA)	--	ACTAVIS ELIZABETH	None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE	078940	005	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE;ORAL	60MG	No	No	2012/05/11 (TA)	--	ACTAVIS ELIZABETH	None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE	078940	006	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE;ORAL	80MG	No	No	2012/05/11 (TA)	--	ACTAVIS ELIZABETH	None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE	078940	007	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE;ORAL	100MG	No	No	2012/05/11 (TA)	--	ACTAVIS ELIZABETH	None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE	079020	001	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE; ORAL	10MG	No	No	2012/05/11 (TA)	--	SUN PHARMA GLOBAL	None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE	079020	002	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE; ORAL	18MG	No	No	2012/05/11 (TA)	--	SUN PHARMA GLOBAL	None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE	079020	003	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE; ORAL	25MG	No	No	2012/05/11 (TA)	--	SUN PHARMA GLOBAL	None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE	079020	004	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE; ORAL	40MG	No	No	2012/05/11 (TA)	--	SUN PHARMA GLOBAL	None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE	079020	005	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE; ORAL	60MG	No	No	2012/05/11 (TA)	--	SUN PHARMA GLOBAL	None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE	079020	006	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE; ORAL	80MG	No	No	2012/05/11 (TA)	--	SUN PHARMA GLOBAL	None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE	079020	007	ANDA	ATOMOXETINE HYDROCHLORIDE	CAPSULE; ORAL	100MG	No	No	2012/05/11 (TA)	--	SUN PHARMA GLOBAL	None (Tentative Approval)