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
MILTOWN	009698	002	NDA	MEPROBAMATE	TABLET;ORAL	400MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1955/04/28	Approved Prior to Jan 1, 1982	MEDPOINTE PHARM HLC	Discontinued
MILTOWN	009698	004	NDA	MEPROBAMATE	TABLET;ORAL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1955/04/28	Approved Prior to Jan 1, 1982	MEDPOINTE PHARM HLC	Discontinued
MILTOWN	083919	001	ANDA	MEPROBAMATE	TABLET;ORAL	600MG	No	No	1974/01/28	Approved Prior to Jan 1, 1982	MEDPOINTE PHARM HLC	Discontinued