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
PROZAC	018936	001	NDA	FLUOXETINE HYDROCHLORIDE	CAPSULE;ORAL	EQ 20MG BASE	Yes	No	1987/12/29	1987/12/29	ELI LILLY AND CO	Prescription
PROZAC	018936	003	NDA	FLUOXETINE HYDROCHLORIDE	CAPSULE;ORAL	EQ 40MG BASE	Yes	Yes	1987/12/29	1999/06/15	ELI LILLY AND CO	Prescription
PROZAC	018936	004	NDA	FLUOXETINE HYDROCHLORIDE	CAPSULE;ORAL	EQ 60MG BASE	No	No	1987/12/29	1999/06/15	ELI LILLY AND CO	Discontinued
PROZAC	018936	006	NDA	FLUOXETINE HYDROCHLORIDE	CAPSULE;ORAL	EQ 10MG BASE	Yes	No	1987/12/29	1992/12/23	ELI LILLY AND CO	Prescription
PROZAC	020101	001	NDA	FLUOXETINE HYDROCHLORIDE	SOLUTION;ORAL	EQ 20MG BASE/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1991/04/24	1991/04/24	LILLY	Discontinued
PROZAC	020974	001	NDA	FLUOXETINE HYDROCHLORIDE	TABLET;ORAL	EQ 10MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1999/03/09	1999/03/09	LILLY	Discontinued
PROZAC	020974	002	NDA	FLUOXETINE HYDROCHLORIDE	TABLET;ORAL	EQ 20MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1999/03/09	1999/03/09	LILLY	Discontinued
PROZAC WEEKLY	021235	001	NDA	FLUOXETINE HYDROCHLORIDE	CAPSULE, DELAYED REL PELLETS;ORAL	EQ 90MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	2001/02/26	2001/02/26	LILLY	Discontinued