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
LIBRIUM	012249	001	NDA	CHLORDIAZEPOXIDE HYDROCHLORIDE	CAPSULE;ORAL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1960/02/24	Approved Prior to Jan 1, 1982	VALEANT PHARM INTL	Discontinued
LIBRIUM	012249	002	NDA	CHLORDIAZEPOXIDE HYDROCHLORIDE	CAPSULE;ORAL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1960/02/24	Approved Prior to Jan 1, 1982	VALEANT PHARM INTL	Discontinued
LIBRIUM	012249	003	NDA	CHLORDIAZEPOXIDE HYDROCHLORIDE	CAPSULE;ORAL	25MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1960/02/24	Approved Prior to Jan 1, 1982	VALEANT PHARM INTL	Discontinued
LIBRIUM	012301	001	NDA	CHLORDIAZEPOXIDE HYDROCHLORIDE	INJECTABLE;INJECTION	100MG/AMP	No	No	1961/07/21	Approved Prior to Jan 1, 1982	BAUSCH	Discontinued
LIBRIUM	085461	001	ANDA	CHLORDIAZEPOXIDE HYDROCHLORIDE	CAPSULE;ORAL	5MG	Yes	No	1977/09/21	Approved Prior to Jan 1, 1982	VALEANT PHARM INTL	Prescription
LIBRIUM	085472	001	ANDA	CHLORDIAZEPOXIDE HYDROCHLORIDE	CAPSULE;ORAL	10MG	Yes	No	1977/09/21	Approved Prior to Jan 1, 1982	VALEANT PHARM INTL	Prescription
LIBRIUM	085475	001	ANDA	CHLORDIAZEPOXIDE HYDROCHLORIDE	CAPSULE;ORAL	25MG	Yes	No	1977/09/21	Approved Prior to Jan 1, 1982	BAUSCH	Prescription