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
VALACYCLOVIR HYDROCHLORIDE	090370	001	ANDA	VALACYCLOVIR HYDROCHLORIDE	TABLET;ORAL	EQ 500MG BASE	No	No	2011/03/16	2011/03/16	WATSON LABS INC	Discontinued
VALACYCLOVIR HYDROCHLORIDE	090370	002	ANDA	VALACYCLOVIR HYDROCHLORIDE	TABLET;ORAL	EQ 1GM BASE	No	No	2011/03/16	2011/03/16	WATSON LABS INC	Discontinued
VALACYCLOVIR HYDROCHLORIDE	201506	001	ANDA	VALACYCLOVIR HYDROCHLORIDE	TABLET;ORAL	EQ 500MG BASE	No	No	2012/04/03	2012/04/03	JUBILANT GENERICS	Prescription
VALACYCLOVIR HYDROCHLORIDE	201506	002	ANDA	VALACYCLOVIR HYDROCHLORIDE	TABLET;ORAL	EQ 1GM BASE	No	No	2012/04/03	2012/04/03	JUBILANT GENERICS	Prescription
VALACYCLOVIR HYDROCHLORIDE	090500	001	ANDA	VALACYCLOVIR HYDROCHLORIDE	TABLET;ORAL	EQ 500MG BASE	No	No	2014/04/04	2014/04/04	APOTEX	Prescription
VALACYCLOVIR HYDROCHLORIDE	090500	002	ANDA	VALACYCLOVIR HYDROCHLORIDE	TABLET;ORAL	EQ 1GM BASE	No	No	2014/04/04	2014/04/04	APOTEX	Prescription
VALACYCLOVIR HYDROCHLORIDE	203047	001	ANDA	VALACYCLOVIR HYDROCHLORIDE	TABLET;ORAL	EQ 500MG BASE	No	No	2015/04/08	2015/04/08	HETERO LABS LTD V	Prescription
VALACYCLOVIR HYDROCHLORIDE	203047	002	ANDA	VALACYCLOVIR HYDROCHLORIDE	TABLET;ORAL	EQ 1GM BASE	No	No	2015/04/08	2015/04/08	HETERO LABS LTD V	Prescription
VALACYCLOVIR HYDROCHLORIDE	079137	001	ANDA	VALACYCLOVIR HYDROCHLORIDE	TABLET;ORAL	EQ 500MG BASE	No	No	2017/12/29	2017/12/29	ZYDUS LIFESCIENCES	Prescription
VALACYCLOVIR HYDROCHLORIDE	079137	002	ANDA	VALACYCLOVIR HYDROCHLORIDE	TABLET;ORAL	EQ 1GM BASE	No	No	2017/12/29	2017/12/29	ZYDUS LIFESCIENCES	Prescription
VALACYCLOVIR HYDROCHLORIDE	209553	001	ANDA	VALACYCLOVIR HYDROCHLORIDE	TABLET;ORAL	EQ 500MG BASE	No	No	2020/03/18	2020/03/18	YILING	Prescription
VALACYCLOVIR HYDROCHLORIDE	209553	002	ANDA	VALACYCLOVIR HYDROCHLORIDE	TABLET;ORAL	EQ 1GM BASE	No	No	2020/03/18	2020/03/18	YILING	Prescription