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
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE	077483	001	ANDA	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	TABLET;ORAL	5MG;6.25MG	No	No	2005/09/08	2005/09/08	SUN PHARM INDS LTD	Discontinued
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE	077483	002	ANDA	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	TABLET;ORAL	10MG;12.5MG	No	No	2005/09/08	2005/09/08	SUN PHARM INDS LTD	Discontinued
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE	077483	003	ANDA	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	TABLET;ORAL	20MG;12.5MG	No	No	2005/09/08	2005/09/08	SUN PHARM INDS LTD	Discontinued
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE	077483	004	ANDA	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	TABLET;ORAL	20MG;25MG	No	No	2005/09/08	2005/09/08	SUN PHARM INDS LTD	Discontinued
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE	078794	001	ANDA	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	TABLET;ORAL	5MG;6.25MG	No	No	2014/08/21	2014/08/21	APOTEX	Prescription
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE	078794	002	ANDA	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	TABLET;ORAL	10MG;12.5MG	No	No	2014/08/21	2014/08/21	APOTEX	Prescription
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE	078794	003	ANDA	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	TABLET;ORAL	20MG;12.5MG	No	No	2014/08/21	2014/08/21	APOTEX	Prescription
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE	078794	004	ANDA	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	TABLET;ORAL	20MG;25MG	No	No	2014/08/21	2014/08/21	APOTEX	Prescription