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
SINEMET	017555	001	NDA	CARBIDOPA; LEVODOPA	TABLET;ORAL	10MG;100MG	Yes	No	1975/05/02	Approved Prior to Jan 1, 1982	ORGANON	Prescription
SINEMET	017555	002	NDA	CARBIDOPA; LEVODOPA	TABLET;ORAL	25MG;250MG	Yes	No	1975/05/02	Approved Prior to Jan 1, 1982	ORGANON	Prescription
SINEMET	017555	003	NDA	CARBIDOPA; LEVODOPA	TABLET;ORAL	25MG;100MG	Yes	No	1975/05/02	Approved Prior to Jan 1, 1982	ORGANON	Prescription
SINEMET CR	019856	001	NDA	CARBIDOPA; LEVODOPA	TABLET, EXTENDED RELEASE;ORAL	50MG;200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1991/05/30	1991/05/30	ORGANON LLC	Discontinued
SINEMET CR	019856	002	NDA	CARBIDOPA; LEVODOPA	TABLET, EXTENDED RELEASE;ORAL	25MG;100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1991/05/30	1992/12/24	ORGANON LLC	Discontinued