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
CIPRO	019537	001	NDA	CIPROFLOXACIN HYDROCHLORIDE	TABLET;ORAL	EQ 100MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1987/10/22	1996/04/08	BAYER HLTHCARE	Discontinued
CIPRO	019537	002	NDA	CIPROFLOXACIN HYDROCHLORIDE	TABLET;ORAL	EQ 250MG BASE	Yes	No	1987/10/22	1987/10/22	BAYER HLTHCARE	Prescription
CIPRO	019537	003	NDA	CIPROFLOXACIN HYDROCHLORIDE	TABLET;ORAL	EQ 500MG BASE	Yes	Yes	1987/10/22	1987/10/22	BAYER HLTHCARE	Prescription
CIPRO	019537	004	NDA	CIPROFLOXACIN HYDROCHLORIDE	TABLET;ORAL	EQ 750MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1987/10/22	1987/10/22	BAYER HLTHCARE	Discontinued
CIPRO	019847	001	NDA	CIPROFLOXACIN	INJECTABLE;INJECTION	400MG/40ML (10MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1990/12/26	1990/12/26	BAYER HLTHCARE	Discontinued
CIPRO	019847	002	NDA	CIPROFLOXACIN	INJECTABLE;INJECTION	200MG/20ML (10MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1990/12/26	1990/12/26	BAYER HLTHCARE	Discontinued
CIPRO	019847	003	NDA	CIPROFLOXACIN	INJECTABLE;INJECTION	1200MG/120ML (10MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1990/12/26	1990/12/26	BAYER HLTHCARE	Discontinued
CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER	019857	001	NDA	CIPROFLOXACIN	INJECTABLE;INJECTION	200MG/100ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1990/12/26	1990/12/26	BAYER HLTHCARE	Discontinued
CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER	019857	002	NDA	CIPROFLOXACIN	INJECTABLE;INJECTION	400MG/200ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1990/12/26	1990/12/26	BAYER HLTHCARE	Discontinued
CIPRO IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	019858	001	NDA	CIPROFLOXACIN	INJECTABLE;INJECTION	200MG/100ML	No	No	1990/12/26	1990/12/26	BAYER PHARMS	Discontinued
CIPRO	020780	001	NDA	CIPROFLOXACIN	FOR SUSPENSION;ORAL	250MG/5ML	Yes	No	1997/09/26	1997/09/26	BAYER HLTHCARE	Prescription
CIPRO	020780	002	NDA	CIPROFLOXACIN	FOR SUSPENSION;ORAL	500MG/5ML	Yes	Yes	1997/09/26	1997/09/26	BAYER HLTHCARE	Prescription
CIPRO HC	020805	001	NDA	CIPROFLOXACIN HYDROCHLORIDE; HYDROCORTISONE	SUSPENSION/DROPS;OTIC	EQ 0.2% BASE;1%	Yes	Yes	1998/02/10	1998/02/10	SANDOZ	Prescription
CIPROFLOXACIN HYDROCHLORIDE	076136	001	ANDA	CIPROFLOXACIN HYDROCHLORIDE	TABLET;ORAL	EQ 250MG BASE	No	No	2001/12/26 (TA)	2004/06/09	TEVA	Discontinued
CIPROFLOXACIN HYDROCHLORIDE	076136	002	ANDA	CIPROFLOXACIN HYDROCHLORIDE	TABLET;ORAL	EQ 500MG BASE	No	No	2001/12/26 (TA)	2004/06/09	TEVA	Discontinued
CIPROFLOXACIN HYDROCHLORIDE	076136	003	ANDA	CIPROFLOXACIN HYDROCHLORIDE	TABLET;ORAL	EQ 750MG BASE	No	No	2001/12/26 (TA)	2004/06/09	TEVA	Discontinued
CIPRO XR	021473	001	NDA	CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	212.6MG;EQ 287.5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	2002/12/13	2002/12/13	BAYER HLTHCARE	Discontinued
CIPRO XR	021473	002	NDA	CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	425.2MG;EQ 574.9MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	2002/12/13	2003/08/28	BAYER HLTHCARE	Discontinued
CIPRODEX	021537	001	NDA	CIPROFLOXACIN; DEXAMETHASONE	SUSPENSION/DROPS;OTIC	0.3%;0.1%	Yes	Yes	2003/07/18	2003/07/18	SANDOZ	Prescription
CIPRO XR	021554	001	NDA	CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE; ORAL	212.6MG; EQ 287.5MG BASE	No	No	2003/08/28	--	BAYER PHARMS	Prescription