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
CLONIDINE HYDROCHLORIDE	209686	001	ANDA	CLONIDINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	0.1MG	No	Yes	2017/11/20	2017/11/20	AJANTA PHARMA LTD	Prescription
CLONIDINE HYDROCHLORIDE	209757	001	ANDA	CLONIDINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	0.1MG	No	No	2017/11/20	2017/11/20	XIAMEN LP PHARM CO	Prescription
CLONIDINE HYDROCHLORIDE	210052	001	ANDA	CLONIDINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	0.1MG	No	No	2017/11/20	2017/11/20	AMNEAL PHARMS NY	Discontinued
CLONIDINE HYDROCHLORIDE	210338	001	ANDA	CLONIDINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	0.1MG	No	No	2018/01/29	2018/01/29	JUBILANT GENERICS	Prescription
CLONIDINE HYDROCHLORIDE	210680	001	ANDA	CLONIDINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	0.1MG	No	No	2018/04/30	2018/04/30	RUBICON RESEARCH	Discontinued
CLONIDINE HYDROCHLORIDE	211433	001	ANDA	CLONIDINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	0.1MG	No	No	2018/10/12	2018/10/12	SOMERSET THERAPS LLC	Prescription
CLONIDINE HYDROCHLORIDE	209675	001	ANDA	CLONIDINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	0.1MG	No	No	2019/03/05	2019/03/05	NOVAST LABS	Prescription