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
CATAPRES	017407	001	NDA	CLONIDINE HYDROCHLORIDE	TABLET;ORAL	0.1MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1974/09/03	Approved Prior to Jan 1, 1982	BOEHRINGER INGELHEIM	Discontinued
CATAPRES	017407	002	NDA	CLONIDINE HYDROCHLORIDE	TABLET;ORAL	0.2MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1974/09/03	Approved Prior to Jan 1, 1982	BOEHRINGER INGELHEIM	Discontinued
CATAPRES	017407	003	NDA	CLONIDINE HYDROCHLORIDE	TABLET;ORAL	0.3MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1974/09/03	Approved Prior to Jan 1, 1982	BOEHRINGER INGELHEIM	Discontinued
CATAPRES-TTS-1	018891	001	NDA	CLONIDINE	SYSTEM;TRANSDERMAL	0.1MG/24HR	Yes	No	1984/10/10	1984/10/10	LAVIPHARM	Prescription
CATAPRES-TTS-2	018891	002	NDA	CLONIDINE	SYSTEM;TRANSDERMAL	0.2MG/24HR	Yes	No	1984/10/10	1984/10/10	LAVIPHARM	Prescription
CATAPRES-TTS-3	018891	003	NDA	CLONIDINE	SYSTEM;TRANSDERMAL	0.3MG/24HR	Yes	Yes	1984/10/10	1984/10/10	LAVIPHARM	Prescription