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
VOLTAREN	019201	001	NDA	DICLOFENAC SODIUM	TABLET, DELAYED RELEASE;ORAL	25MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1988/07/28	1988/07/28	NOVARTIS	Discontinued
VOLTAREN	019201	002	NDA	DICLOFENAC SODIUM	TABLET, DELAYED RELEASE;ORAL	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1988/07/28	1988/07/28	NOVARTIS	Discontinued
VOLTAREN	019201	003	NDA	DICLOFENAC SODIUM	TABLET, DELAYED RELEASE;ORAL	75MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1988/07/28	1988/07/28	NOVARTIS	Discontinued
VOLTAREN	020037	001	NDA	DICLOFENAC SODIUM	SOLUTION/DROPS;OPHTHALMIC	0.1%	Yes	No	1991/03/28	1991/03/28	NOVARTIS	Discontinued
VOLTAREN-XR	020254	001	NDA	DICLOFENAC SODIUM	TABLET, EXTENDED RELEASE;ORAL	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1996/03/08	1996/03/08	NOVARTIS	Discontinued
VOLTAREN ARTHRITIS PAIN	022122	001	NDA	DICLOFENAC SODIUM	GEL;TOPICAL	1%	Yes	Yes	2007/10/17	2007/10/17	HALEON US HOLDINGS	Over-the-counter