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
ZOVIRAX	018604	001	NDA	ACYCLOVIR	OINTMENT;TOPICAL	5%	Yes	Yes	1982/03/29	1982/03/29	BAUSCH	Prescription
ZOVIRAX	018603	001	NDA	ACYCLOVIR SODIUM	INJECTABLE;INJECTION	EQ 500MG BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1982/10/22	1982/10/22	GLAXOSMITHKLINE	Discontinued
ZOVIRAX	018603	002	NDA	ACYCLOVIR SODIUM	INJECTABLE;INJECTION	EQ 1GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1982/10/22	1989/06/29	GLAXOSMITHKLINE	Discontinued
ZOVIRAX	018603	003	NDA	ACYCLOVIR SODIUM	INJECTABLE;INJECTION	EQ 250MG BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1982/10/22	1983/08/30	GLAXOSMITHKLINE	Discontinued
ZOVIRAX	018828	001	NDA	ACYCLOVIR	CAPSULE;ORAL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1985/01/25	1985/01/25	NORVIUM BIOSCIENCE	Discontinued
ZOVIRAX	019909	001	NDA	ACYCLOVIR	SUSPENSION;ORAL	200MG/5ML	Yes	No	1989/12/22	1989/12/22	NORVIUM BIOSCIENCE	Discontinued
ZOVIRAX	020089	001	NDA	ACYCLOVIR	TABLET;ORAL	400MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1991/04/30	1991/04/30	NORVIUM BIOSCIENCE	Discontinued
ZOVIRAX	020089	002	NDA	ACYCLOVIR	TABLET;ORAL	800MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1991/04/30	1991/04/30	NORVIUM BIOSCIENCE	Discontinued
ZOVIRAX	021478	001	NDA	ACYCLOVIR	CREAM;TOPICAL	5%	Yes	No	2002/12/30	2002/12/30	BAUSCH	Prescription