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
SOLODYN	050808	001	NDA	MINOCYCLINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	EQ 45MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	2006/05/08	2006/05/08	BAUSCH	Discontinued
SOLODYN	050808	002	NDA	MINOCYCLINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	EQ 90MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	2006/05/08	2006/05/08	BAUSCH	Discontinued
SOLODYN	050808	003	NDA	MINOCYCLINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	EQ 135MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	2006/05/08	2006/05/08	BAUSCH	Discontinued
SOLODYN	050808	004	NDA	MINOCYCLINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	EQ 65MG BASE	Yes	No	2006/05/08	2009/07/23	BAUSCH	Prescription
SOLODYN	050808	005	NDA	MINOCYCLINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	EQ 115MG BASE	Yes	Yes	2006/05/08	2009/07/23	BAUSCH	Prescription
SOLODYN	050808	006	NDA	MINOCYCLINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	EQ 105MG BASE	Yes	No	2006/05/08	2010/08/27	BAUSCH	Prescription
SOLODYN	050808	007	NDA	MINOCYCLINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	EQ 80MG BASE	Yes	No	2006/05/08	2010/08/27	BAUSCH	Prescription
SOLODYN	050808	008	NDA	MINOCYCLINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE;ORAL	EQ 55MG BASE	Yes	No	2006/05/08	2010/08/27	BAUSCH	Prescription