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
VISTARIL	011111	001	NDA	HYDROXYZINE HYDROCHLORIDE	INJECTABLE;INJECTION	25MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1957/09/18	Approved Prior to Jan 1, 1982	PFIZER	Discontinued
VISTARIL	011111	002	NDA	HYDROXYZINE HYDROCHLORIDE	INJECTABLE;INJECTION	50MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1957/09/18	Approved Prior to Jan 1, 1982	PFIZER	Discontinued
VISTARIL	011795	001	NDA	HYDROXYZINE PAMOATE	SUSPENSION;ORAL	EQ 25MG HYDROCHLORIDE/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1959/06/03	Approved Prior to Jan 1, 1982	PFIZER	Discontinued
VISTARIL	011459	002	NDA	HYDROXYZINE PAMOATE	CAPSULE;ORAL	EQ 25MG HYDROCHLORIDE	Yes	No	1968/11/15	Approved Prior to Jan 1, 1982	PFIZER	Prescription
VISTARIL	011459	004	NDA	HYDROXYZINE PAMOATE	CAPSULE;ORAL	EQ 50MG HYDROCHLORIDE	Yes	No	1968/11/15	Approved Prior to Jan 1, 1982	PFIZER	Prescription
VISTARIL	011459	006	NDA	HYDROXYZINE PAMOATE	CAPSULE;ORAL	EQ 100MG HYDROCHLORIDE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1968/11/15	Approved Prior to Jan 1, 1982	PFIZER	Discontinued