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
HYPAQUE	009561	001	NDA	DIATRIZOATE SODIUM	INJECTABLE;INJECTION	50%	No	No	1954/11/26	Approved Prior to Jan 1, 1982	GE HEALTHCARE	Discontinued
HYPAQUE SODIUM 20%	009561	002	NDA	DIATRIZOATE SODIUM	SOLUTION;URETERAL	20%	No	No	1954/11/26	Approved Prior to Jan 1, 1982	GE HEALTHCARE	Discontinued
HYPAQUE	009561	003	NDA	DIATRIZOATE SODIUM	INJECTABLE;INJECTION	25%	No	No	1954/11/26	Approved Prior to Jan 1, 1982	GE HEALTHCARE	Discontinued
HYPAQUE-M,90%	010220	002	NDA	DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM	INJECTABLE;INJECTION	60%;30%	No	No	1955/11/09	Approved Prior to Jan 1, 1982	GE HEALTHCARE	Discontinued
HYPAQUE-M,75%	010220	003	NDA	DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM	INJECTABLE;INJECTION	50%;25%	No	No	1955/11/09	Approved Prior to Jan 1, 1982	GE HEALTHCARE	Discontinued
HYPAQUE	011386	001	NDA	DIATRIZOATE SODIUM	FOR SOLUTION;ORAL, RECTAL	100%	No	No	1956/03/26	Approved Prior to Jan 1, 1982	GE HEALTHCARE	Discontinued
HYPAQUE	011386	003	NDA	DIATRIZOATE SODIUM	SOLUTION;ORAL, RECTAL	40%	No	No	1956/03/26	Approved Prior to Jan 1, 1982	GE HEALTHCARE	Discontinued
HYPAQUE	016403	001	NDA	DIATRIZOATE MEGLUMINE	INJECTABLE;INJECTION	60%	No	No	1969/08/21	Approved Prior to Jan 1, 1982	GE HEALTHCARE	Discontinued
HYPAQUE	016403	002	NDA	DIATRIZOATE MEGLUMINE	INJECTABLE;INJECTION	30%	No	No	1969/08/21	Approved Prior to Jan 1, 1982	GE HEALTHCARE	Discontinued
HYPAQUE-CYSTO	016403	003	NDA	DIATRIZOATE MEGLUMINE	SOLUTION;URETHRAL	30%	No	No	1969/08/21	Approved Prior to Jan 1, 1982	GE HEALTHCARE	Discontinued
HYPAQUE-76	086505	001	ANDA	DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM	INJECTABLE;INJECTION	66%;10%	No	No	1980/07/02	Approved Prior to Jan 1, 1982	GE HEALTHCARE	Discontinued