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
ISUPREL	006327	002	NDA	ISOPROTERENOL HYDROCHLORIDE	SOLUTION;INHALATION	0.5%	No	No	--	Approved Prior to Jan 1, 1982	SANOFI AVENTIS US	Discontinued
ISUPREL	006327	003	NDA	ISOPROTERENOL HYDROCHLORIDE	SOLUTION;INHALATION	1%	No	No	--	Approved Prior to Jan 1, 1982	SANOFI AVENTIS US	Discontinued
ISUPREL	011178	001	NDA	ISOPROTERENOL HYDROCHLORIDE	AEROSOL, METERED;INHALATION	0.103MG/INH	No	No	--	Approved Prior to Jan 1, 1982	SANOFI AVENTIS US	Discontinued
ISUPREL	006328	001	NDA	ISOPROTERENOL HYDROCHLORIDE	TABLET;RECTAL, SUBLINGUAL	10MG	No	No	1948/02/19	Approved Prior to Jan 1, 1982	SANOFI AVENTIS US	Discontinued
ISUPREL	006328	002	NDA	ISOPROTERENOL HYDROCHLORIDE	TABLET;RECTAL, SUBLINGUAL	15MG	No	No	1948/02/19	Approved Prior to Jan 1, 1982	SANOFI AVENTIS US	Discontinued
ISUPREL	010515	001	NDA	ISOPROTERENOL HYDROCHLORIDE	INJECTABLE;INJECTION	0.2MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1956/05/25	Approved Prior to Jan 1, 1982	BAUSCH	Discontinued