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
SINEQUAN	016798	001	NDA	DOXEPIN HYDROCHLORIDE	CAPSULE;ORAL	EQ 25MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1969/09/23	Approved Prior to Jan 1, 1982	PFIZER	Discontinued
SINEQUAN	016798	002	NDA	DOXEPIN HYDROCHLORIDE	CAPSULE;ORAL	EQ 50MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1969/09/23	Approved Prior to Jan 1, 1982	PFIZER	Discontinued
SINEQUAN	016798	003	NDA	DOXEPIN HYDROCHLORIDE	CAPSULE;ORAL	EQ 10MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1969/09/23	Approved Prior to Jan 1, 1982	PFIZER	Discontinued
SINEQUAN	016798	005	NDA	DOXEPIN HYDROCHLORIDE	CAPSULE;ORAL	EQ 100MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1969/09/23	Approved Prior to Jan 1, 1982	PFIZER	Discontinued
SINEQUAN	016798	006	NDA	DOXEPIN HYDROCHLORIDE	CAPSULE;ORAL	EQ 75MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1969/09/23	Approved Prior to Jan 1, 1982	PFIZER	Discontinued
SINEQUAN	016798	007	NDA	DOXEPIN HYDROCHLORIDE	CAPSULE;ORAL	EQ 150MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1969/09/23	Approved Prior to Jan 1, 1982	PFIZER	Discontinued
SINEQUAN	017516	001	NDA	DOXEPIN HYDROCHLORIDE	CONCENTRATE;ORAL	EQ 10MG BASE/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1974/03/11	Approved Prior to Jan 1, 1982	PFIZER	Discontinued