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
DILANTIN-125	008762	001	NDA	PHENYTOIN	SUSPENSION;ORAL	125MG/5ML	Yes	Yes	1953/01/06	Approved Prior to Jan 1, 1982	VIATRIS	Prescription
DILANTIN-30	008762	002	NDA	PHENYTOIN	SUSPENSION;ORAL	30MG/5ML	No	No	1953/01/06	Approved Prior to Jan 1, 1982	VIATRIS	Discontinued
DILANTIN	010151	001	NDA	PHENYTOIN SODIUM	INJECTABLE;INJECTION	50MG/ML	No	No	1956/03/01	Approved Prior to Jan 1, 1982	PARKE DAVIS	Discontinued
DILANTIN	084349	001	ANDA	PHENYTOIN SODIUM	CAPSULE;ORAL	30MG EXTENDED	Yes	Yes	1976/08/27	Approved Prior to Jan 1, 1982	VIATRIS	Prescription
DILANTIN	084349	002	ANDA	PHENYTOIN SODIUM	CAPSULE;ORAL	100MG EXTENDED	Yes	Yes	1976/08/27	Approved Prior to Jan 1, 1982	VIATRIS	Prescription
DILANTIN	084427	001	ANDA	PHENYTOIN	TABLET, CHEWABLE;ORAL	50MG	Yes	Yes	1979/02/26	Approved Prior to Jan 1, 1982	PHARMACIA	Prescription