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
MINOCIN	062139	001	ANDA	MINOCYCLINE HYDROCHLORIDE	INJECTABLE;INJECTION	EQ 100MG BASE/VIAL	No	No	--	Approved Prior to Jan 1, 1982	LEDERLE	Discontinued
MINOCIN	050315	001	NDA	MINOCYCLINE HYDROCHLORIDE	CAPSULE;ORAL	EQ 100MG BASE	No	No	1971/06/30	Approved Prior to Jan 1, 1982	TRIAX PHARMS	Discontinued
MINOCIN	050315	002	NDA	MINOCYCLINE HYDROCHLORIDE	CAPSULE;ORAL	EQ 50MG BASE	No	No	1971/06/30	Approved Prior to Jan 1, 1982	TRIAX PHARMS	Discontinued
MINOCIN	050444	001	NDA	MINOCYCLINE HYDROCHLORIDE	INJECTABLE;INJECTION	EQ 100MG BASE/VIAL	Yes	Yes	1972/10/26	Approved Prior to Jan 1, 1982	REMPEX	Prescription
MINOCIN	050445	001	NDA	MINOCYCLINE HYDROCHLORIDE	SUSPENSION;ORAL	EQ 50MG BASE/5ML	No	No	1972/10/26	Approved Prior to Jan 1, 1982	BAUSCH	Discontinued
MINOCIN	050649	001	NDA	MINOCYCLINE HYDROCHLORIDE	CAPSULE;ORAL	EQ 50MG BASE	Yes	No	1990/05/31	1990/05/31	BAUSCH	Prescription
MINOCIN	050649	002	NDA	MINOCYCLINE HYDROCHLORIDE	CAPSULE;ORAL	EQ 100MG BASE	Yes	No	1990/05/31	1990/05/31	BAUSCH	Prescription
MINOCIN	050649	003	NDA	MINOCYCLINE HYDROCHLORIDE	CAPSULE;ORAL	EQ 75MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1990/05/31	2001/02/12	BAUSCH	Discontinued