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
AMIKIN	050495	001	NDA	AMIKACIN SULFATE	INJECTABLE;INJECTION	EQ 50MG BASE/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	--	Approved Prior to Jan 1, 1982	APOTHECON	Discontinued
AMIKIN	050495	002	NDA	AMIKACIN SULFATE	INJECTABLE;INJECTION	EQ 250MG BASE/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	--	Approved Prior to Jan 1, 1982	APOTHECON	Discontinued
AMIKIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	050618	001	NDA	AMIKACIN SULFATE	INJECTABLE;INJECTION	EQ 10MG BASE/ML	No	No	--	1987/11/30	APOTHECON	Discontinued
AMIKIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	050618	002	NDA	AMIKACIN SULFATE	INJECTABLE;INJECTION	EQ 5MG BASE/ML	No	No	--	1987/11/30	APOTHECON	Discontinued
AMIKIN	062562	001	ANDA	AMIKACIN SULFATE	INJECTABLE;INJECTION	EQ 50MG BASE/ML	No	No	--	1984/09/20	APOTHECON	Discontinued
AMIKIN	062562	002	ANDA	AMIKACIN SULFATE	INJECTABLE;INJECTION	EQ 250MG BASE/ML	No	No	--	1984/09/20	APOTHECON	Discontinued
AMIKIN	062311	001	ANDA	AMIKACIN SULFATE	INJECTABLE;INJECTION	EQ 50MG BASE/ML	No	No	1981/01/22	Approved Prior to Jan 1, 1982	APOTHECON	Discontinued
AMIKIN	062311	002	ANDA	AMIKACIN SULFATE	INJECTABLE;INJECTION	EQ 250MG BASE/ML	No	No	1981/01/22	Approved Prior to Jan 1, 1982	APOTHECON	Discontinued