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
LOTENSIN	019851	001	NDA	BENAZEPRIL HYDROCHLORIDE	TABLET;ORAL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1991/06/25	1991/06/25	VALIDUS PHARMS	Discontinued
LOTENSIN	019851	002	NDA	BENAZEPRIL HYDROCHLORIDE	TABLET;ORAL	10MG	Yes	No	1991/06/25	1991/06/25	VALIDUS PHARMS	Prescription
LOTENSIN	019851	003	NDA	BENAZEPRIL HYDROCHLORIDE	TABLET;ORAL	20MG	Yes	No	1991/06/25	1991/06/25	VALIDUS PHARMS	Prescription
LOTENSIN	019851	004	NDA	BENAZEPRIL HYDROCHLORIDE	TABLET;ORAL	40MG	Yes	No	1991/06/25	1991/06/25	VALIDUS PHARMS	Prescription
LOTENSIN HCT	020033	001	NDA	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	TABLET;ORAL	5MG;6.25MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1992/05/19	1992/05/19	VALIDUS PHARMS	Discontinued
LOTENSIN HCT	020033	002	NDA	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	TABLET;ORAL	10MG;12.5MG	Yes	No	1992/05/19	1992/05/19	VALIDUS PHARMS	Prescription
LOTENSIN HCT	020033	003	NDA	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	TABLET;ORAL	20MG;25MG	Yes	Yes	1992/05/19	1992/05/19	VALIDUS PHARMS	Prescription
LOTENSIN HCT	020033	004	NDA	BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	TABLET;ORAL	20MG;12.5MG	Yes	No	1992/05/19	1992/05/19	VALIDUS PHARMS	Prescription