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
GRIFULVIN V	060618	001	ANDA	GRISEOFULVIN, MICROCRYSTALLINE	TABLET;ORAL	125MG	No	No	1971/07/14	Approved Prior to Jan 1, 1982	J AND J	Discontinued
GRIFULVIN V	060618	002	ANDA	GRISEOFULVIN, MICROCRYSTALLINE	TABLET;ORAL	250MG	No	No	1971/07/14	Approved Prior to Jan 1, 1982	J AND J	Discontinued
GRIFULVIN V	060618	003	ANDA	GRISEOFULVIN, MICROCRYSTALLINE	TABLET;ORAL	500MG	No	No	1971/07/14	Approved Prior to Jan 1, 1982	J AND J	Discontinued
GRIFULVIN V	050448	001	NDA	GRISEOFULVIN, MICROCRYSTALLINE	SUSPENSION;ORAL	125MG/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1972/05/30	Approved Prior to Jan 1, 1982	JOHNSON AND JOHNSON	Discontinued
GRIFULVIN V	062279	001	ANDA	GRISEOFULVIN, MICROCRYSTALLINE	TABLET;ORAL	125MG	No	No	1980/06/02	Approved Prior to Jan 1, 1982	VALEANT LUXEMBOURG	Discontinued
GRIFULVIN V	062279	002	ANDA	GRISEOFULVIN, MICROCRYSTALLINE	TABLET;ORAL	250MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1980/06/02	Approved Prior to Jan 1, 1982	VALEANT LUXEMBOURG	Discontinued
GRIFULVIN V	062279	003	ANDA	GRISEOFULVIN, MICROSIZE	TABLET;ORAL	500MG	No	No	1980/06/02	Approved Prior to Jan 1, 1982	VALEANT LUXEMBOURG	Discontinued
GRIFULVIN V	062483	001	ANDA	GRISEOFULVIN, MICROSIZE	SUSPENSION;ORAL	125MG/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1984/01/26	1984/01/26	VALEANT LUXEMBOURG	Discontinued