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
ALDOMET	013400	001	NDA	METHYLDOPA	TABLET;ORAL	250MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1962/12/20	Approved Prior to Jan 1, 1982	MERCK	Discontinued
ALDOMET	013400	002	NDA	METHYLDOPA	TABLET;ORAL	500MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1962/12/20	Approved Prior to Jan 1, 1982	MERCK	Discontinued
ALDOMET	013400	003	NDA	METHYLDOPA	TABLET;ORAL	125MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1962/12/20	Approved Prior to Jan 1, 1982	MERCK	Discontinued
ALDOMET	013401	001	NDA	METHYLDOPATE HYDROCHLORIDE	INJECTABLE;INJECTION	50MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1962/12/20	Approved Prior to Jan 1, 1982	MERCK	Discontinued
ALDOMET	018389	001	NDA	METHYLDOPA	SUSPENSION;ORAL	250MG/5ML	No	No	1981/08/28	Approved Prior to Jan 1, 1982	MERCK	Discontinued