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
BENTYL	007409	001	NDA	DICYCLOMINE HYDROCHLORIDE	TABLET;ORAL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1950/05/11	1984/10/15	ALLERGAN	Discontinued
BENTYL	007409	003	NDA	DICYCLOMINE HYDROCHLORIDE	CAPSULE;ORAL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1950/05/11	1984/10/15	ALLERGAN	Discontinued
BENTYL	007961	002	NDA	DICYCLOMINE HYDROCHLORIDE	SYRUP;ORAL	10MG/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1951/04/30	1984/10/15	APTALIS PHARMA US	Discontinued
BENTYL	008370	001	NDA	DICYCLOMINE HYDROCHLORIDE	INJECTABLE;INJECTION	10MG/ML	Yes	No	1952/08/13	1984/10/15	ABBVIE	Discontinued
BENTYL PRESERVATIVE FREE	008370	002	NDA	DICYCLOMINE HYDROCHLORIDE	INJECTABLE;INJECTION	10MG/ML	Yes	No	1952/08/13	1984/10/15	ABBVIE	Discontinued