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
SECONAL SODIUM	086530	001	ANDA	SECOBARBITAL SODIUM	SUPPOSITORY;RECTAL	30MG	No	No	--	Approved Prior to Jan 1, 1982	LILLY	Discontinued
SECONAL SODIUM	086530	002	ANDA	SECOBARBITAL SODIUM	SUPPOSITORY;RECTAL	60MG	No	No	--	Approved Prior to Jan 1, 1982	LILLY	Discontinued
SECONAL SODIUM	086530	003	ANDA	SECOBARBITAL SODIUM	SUPPOSITORY;RECTAL	120MG	No	No	--	Approved Prior to Jan 1, 1982	LILLY	Discontinued
SECONAL SODIUM	086530	004	ANDA	SECOBARBITAL SODIUM	SUPPOSITORY;RECTAL	200MG	No	No	--	Approved Prior to Jan 1, 1982	LILLY	Discontinued
SECONAL SODIUM	007392	002	NDA	SECOBARBITAL SODIUM	INJECTABLE;INJECTION	50MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1950/07/19	Approved Prior to Jan 1, 1982	LILLY	Discontinued
SECONAL SODIUM	086101	001	ANDA	SECOBARBITAL SODIUM	CAPSULE;ORAL	50MG	No	No	1983/10/03	1983/10/03	VALEANT PHARMS NORTH	Discontinued
SECONAL SODIUM	086101	002	ANDA	SECOBARBITAL SODIUM	CAPSULE;ORAL	100MG	No	No	1983/10/03	1983/10/03	VALEANT PHARMS NORTH	Discontinued