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
PRO-BANTHINE	008843	001	NDA	PROPANTHELINE BROMIDE	INJECTABLE;INJECTION	30MG/VIAL	No	No	--	Approved Prior to Jan 1, 1982	GD SEARLE LLC	Discontinued
PRO-BANTHINE	008732	002	NDA	PROPANTHELINE BROMIDE	TABLET;ORAL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1953/04/02	Approved Prior to Jan 1, 1982	SHIRE	Discontinued
PRO-BANTHINE	008732	003	NDA	PROPANTHELINE BROMIDE	TABLET;ORAL	7.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1953/04/02	Approved Prior to Jan 1, 1982	SHIRE	Discontinued