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
MYCOSTATIN	060571	001	ANDA	NYSTATIN	OINTMENT;TOPICAL	100,000 UNITS/GM Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	--	Approved Prior to Jan 1, 1982	DELCOR ASSET CORP	Discontinued
MYCOSTATIN	060577	001	ANDA	NYSTATIN	TABLET;VAGINAL	100,000 UNITS	No	No	1964/07/08	Approved Prior to Jan 1, 1982	DELCOR ASSET CORP	Discontinued
MYCOSTATIN	060578	001	ANDA	NYSTATIN	POWDER;TOPICAL	100,000 UNITS/GM Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1964/09/08	Approved Prior to Jan 1, 1982	DELCOR ASSET CORP	Discontinued
MYCOSTATIN	060574	001	ANDA	NYSTATIN	TABLET;ORAL	500,000 UNITS	No	No	1964/09/16	Approved Prior to Jan 1, 1982	DELCOR ASSET CORP	Discontinued
MYCOSTATIN	060575	001	ANDA	NYSTATIN	CREAM;TOPICAL	100,000 UNITS/GM Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1965/02/09	Approved Prior to Jan 1, 1982	DELCOR ASSET CORP	Discontinued
MYCOSTATIN	061533	001	ANDA	NYSTATIN	SUSPENSION;ORAL	100,000 UNITS/ML	No	No	1972/02/25	Approved Prior to Jan 1, 1982	DELCOR ASSET CORP	Discontinued
MYCOSTATIN	050619	001	NDA	NYSTATIN	PASTILLE;ORAL	200,000 UNITS	No	No	1987/04/09	1987/04/09	DELCOR ASSET CORP	Discontinued