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
LACTULOSE	074712	001	ANDA	LACTULOSE	FOR SOLUTION;ORAL	10GM/PACKET	No	Yes	1997/12/10	1997/12/10	CUMBERLAND PHARMS	Prescription
LACTULOSE	074712	002	ANDA	LACTULOSE	FOR SOLUTION;ORAL	20GM/PACKET	No	Yes	1997/12/10	1997/12/10	CUMBERLAND PHARMS	Prescription
LACTULOSE	075993	001	ANDA	LACTULOSE	SOLUTION;ORAL	10GM/15ML	No	No	2001/07/26	2001/07/26	LANNETT CO INC	Prescription
LACTULOSE	075911	001	ANDA	LACTULOSE	SOLUTION;ORAL	10GM/15ML	No	No	2002/02/21	2002/02/21	XTTRIUM LABS INC	Prescription
LACTULOSE	076645	001	ANDA	LACTULOSE	SOLUTION;ORAL, RECTAL	10GM/15ML	No	No	2003/07/28	2003/07/28	BAJAJ	Prescription
LACTULOSE	078430	001	ANDA	LACTULOSE	SOLUTION;ORAL	10GM/15ML	No	No	2007/11/28	2007/11/28	ANI PHARMS	Discontinued
LACTULOSE	090426	001	ANDA	LACTULOSE	SOLUTION;ORAL, RECTAL	10GM/15ML	No	No	2008/11/21	2008/11/21	ANI PHARMS	Discontinued
ULORIC	021856	001	NDA	FEBUXOSTAT	TABLET;ORAL	40MG	Yes	No	2009/02/13	2009/02/13	TAKEDA PHARMS USA	Prescription
ULORIC	021856	002	NDA	FEBUXOSTAT	TABLET;ORAL	80MG	Yes	Yes	2009/02/13	2009/02/13	TAKEDA PHARMS USA	Prescription
TAMSULOSIN HYDROCHLORIDE	090377	001	ANDA	TAMSULOSIN HYDROCHLORIDE	CAPSULE;ORAL	0.4MG	No	No	2010/03/02	2010/03/02	IMPAX LABS	Prescription
TAMSULOSIN HYDROCHLORIDE	077630	001	ANDA	TAMSULOSIN HYDROCHLORIDE	CAPSULE;ORAL	0.4MG	No	No	2010/04/27	2010/04/27	TEVA PHARMS	Prescription
TAMSULOSIN HYDROCHLORIDE	078015	001	ANDA	TAMSULOSIN HYDROCHLORIDE	CAPSULE;ORAL	0.4MG	No	No	2010/04/27	2010/04/27	SANDOZ	Prescription
TAMSULOSIN HYDROCHLORIDE	078225	001	ANDA	TAMSULOSIN HYDROCHLORIDE	CAPSULE;ORAL	0.4MG	No	No	2010/04/27	2010/04/27	ZYDUS PHARMS USA INC	Prescription
TAMSULOSIN HYDROCHLORIDE	078801	001	ANDA	TAMSULOSIN HYDROCHLORIDE	CAPSULE;ORAL	0.4MG	No	No	2010/04/27	2010/04/27	SYNTHON PHARMS	Prescription
TAMSULOSIN HYDROCHLORIDE	078938	001	ANDA	TAMSULOSIN HYDROCHLORIDE	CAPSULE;ORAL	0.4MG	No	No	2010/04/27	2010/04/27	WOCKHARDT	Prescription
TAMSULOSIN HYDROCHLORIDE	090408	001	ANDA	TAMSULOSIN HYDROCHLORIDE	CAPSULE;ORAL	0.4MG	No	No	2010/04/27	2010/04/27	NORVIUM BIOSCIENCE	Discontinued
TAMSULOSIN HYDROCHLORIDE	090931	001	ANDA	TAMSULOSIN HYDROCHLORIDE	CAPSULE;ORAL	0.4MG	No	No	2010/07/15	2010/07/15	SUN PHARM INDS LTD	Prescription
DULOXETINE HYDROCHLORIDE	090669	001	ANDA	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE; ORAL	EQ 20MG BASE	No	No	2010/11/18 (TA)	--	IMPAX LABS INC	None (Tentative Approval)
DULOXETINE HYDROCHLORIDE	090669	002	ANDA	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE; ORAL	EQ 30MG BASE	No	No	2010/11/18 (TA)	--	IMPAX LABS INC	None (Tentative Approval)
DULOXETINE HYDROCHLORIDE	090669	003	ANDA	DULOXETINE HYDROCHLORIDE	CAPSULE, DELAYED RELEASE; ORAL	EQ 60MG BASE	No	No	2010/11/18 (TA)	--	IMPAX LABS INC	None (Tentative Approval)