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
MEGACE	016979	001	NDA	MEGESTROL ACETATE	TABLET;ORAL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1971/08/18	Approved Prior to Jan 1, 1982	BRISTOL MYERS SQUIBB	Discontinued
MEGACE	016979	002	NDA	MEGESTROL ACETATE	TABLET;ORAL	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1971/08/18	Approved Prior to Jan 1, 1982	BRISTOL MYERS SQUIBB	Discontinued
MEGACE	020264	001	NDA	MEGESTROL ACETATE	SUSPENSION;ORAL	40MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1993/09/10	1993/09/10	BRISTOL MYERS SQUIBB	Discontinued
MEGACE ES	021778	001	NDA	MEGESTROL ACETATE	SUSPENSION;ORAL	125MG/ML	Yes	Yes	2005/07/05	2005/07/05	ENDO PHARMS INC	Prescription