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
TEGRETOL	016608	001	NDA	CARBAMAZEPINE	TABLET;ORAL	200MG	Yes	Yes	1968/03/11	Approved Prior to Jan 1, 1982	NOVARTIS	Prescription
TEGRETOL	018281	001	NDA	CARBAMAZEPINE	TABLET, CHEWABLE;ORAL	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1981/12/14	Approved Prior to Jan 1, 1982	NOVARTIS	Discontinued
TEGRETOL	018927	001	NDA	CARBAMAZEPINE	SUSPENSION;ORAL	100MG/5ML	Yes	Yes	1987/12/18	1987/12/18	NOVARTIS	Prescription
TEGRETOL-XR	020234	001	NDA	CARBAMAZEPINE	TABLET, EXTENDED RELEASE;ORAL	100MG	Yes	No	1996/03/25	1996/03/25	NOVARTIS	Prescription
TEGRETOL-XR	020234	002	NDA	CARBAMAZEPINE	TABLET, EXTENDED RELEASE;ORAL	200MG	Yes	No	1996/03/25	1996/03/25	NOVARTIS	Prescription
TEGRETOL-XR	020234	003	NDA	CARBAMAZEPINE	TABLET, EXTENDED RELEASE;ORAL	400MG	Yes	Yes	1996/03/25	1996/03/25	NOVARTIS	Prescription