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
FEXOFENADINE HYDROCHLORIDE HIVES	076502	007	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET;ORAL	60MG	No	No	2006/04/11	2011/04/12	DR REDDYS LABS LTD	Over-the-counter
FEXOFENADINE HYDROCHLORIDE ALLERGY	076502	008	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET;ORAL	180MG	No	No	2006/04/11	2011/04/12	DR REDDYS LABS LTD	Over-the-counter
FEXOFENADINE HYDROCHLORIDE HIVES	076502	009	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET;ORAL	180MG	No	No	2006/04/11	2011/04/12	DR REDDYS LABS LTD	Over-the-counter
FEXOFENADINE HYDROCHLORIDE	077081	001	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET;ORAL	180MG	No	No	2007/04/16	2007/04/16	RISING	Prescription
FEXOFENADINE HYDROCHLORIDE	077081	002	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET;ORAL	30MG	No	No	2007/04/16	2008/04/11	RISING	Discontinued
FEXOFENADINE HYDROCHLORIDE	077081	003	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET;ORAL	60MG	No	No	2007/04/16	2008/04/11	RISING	Prescription
CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGY	077081	004	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET;ORAL	30MG	No	No	2007/04/16	2011/07/21	RISING	Discontinued
CHILDREN'S FEXOFENADINE HYDROCHLORIDE HIVES	077081	005	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET;ORAL	30MG	No	No	2007/04/16	2011/07/21	RISING	Discontinued
FEXOFENADINE HYDROCHLORIDE ALLERGY	077081	006	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET;ORAL	60MG	No	No	2007/04/16	2011/07/21	RISING	Over-the-counter
FEXOFENADINE HYDROCHLORIDE HIVES	077081	007	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET;ORAL	60MG	No	No	2007/04/16	2011/07/21	RISING	Over-the-counter
FEXOFENADINE HYDROCHLORIDE ALLERGY	077081	008	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET;ORAL	180MG	No	No	2007/04/16	2011/07/21	RISING	Over-the-counter
FEXOFENADINE HYDROCHLORIDE HIVES	077081	009	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET;ORAL	180MG	No	No	2007/04/16	2011/07/21	RISING	Over-the-counter
FEXOFENADINE HYDROCHLORIDE	076970	001	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET; ORAL	30MG	No	No	2007/05/16 (TA)	--	RANBAXY	None (Tentative Approval)
FEXOFENADINE HYDROCHLORIDE	076970	002	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET; ORAL	60MG	No	No	2007/05/16 (TA)	--	RANBAXY	None (Tentative Approval)
FEXOFENADINE HYDROCHLORIDE	076970	003	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET; ORAL	180MG	No	No	2007/05/16 (TA)	--	RANBAXY	None (Tentative Approval)
FEXOFENADINE HYDROCHLORIDE	076707	001	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET; ORAL	30MG	No	No	2009/04/24 (TA)	--	SANDOZ	None (Tentative Approval)
FEXOFENADINE HYDROCHLORIDE	076707	002	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET; ORAL	60MG	No	No	2009/04/24 (TA)	--	SANDOZ	None (Tentative Approval)
FEXOFENADINE HYDROCHLORIDE	076707	003	ANDA	FEXOFENADINE HYDROCHLORIDE	TABLET; ORAL	180MG	No	No	2009/04/24 (TA)	--	SANDOZ	None (Tentative Approval)
FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE	077999	001	ANDA	FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE; ORAL	60MG; 120MG	No	No	2010/02/25 (TA)	--	PLD ACQUISITIONS LLC	None (Tentative Approval)
FEXOFENADINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE	079043	002	ANDA	FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	180MG;240MG	No	No	2010/03/17	2011/06/22	DR REDDYS LABS LTD	Over-the-counter