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
DELALUTIN	010347	002	NDA	HYDROXYPROGESTERONE CAPROATE	SOLUTION;INTRAMUSCULAR	250MG/ML (250MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	--	Approved Prior to Jan 1, 1982	BRISTOL MYERS SQUIBB	Discontinued
DELALUTIN	010347	004	NDA	HYDROXYPROGESTERONE CAPROATE	SOLUTION;INTRAMUSCULAR	125MG/ML (125MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	--	Approved Prior to Jan 1, 1982	BRISTOL MYERS SQUIBB	Discontinued
DELALUTIN	016911	001	NDA	HYDROXYPROGESTERONE CAPROATE	SOLUTION;INTRAMUSCULAR	125MG/ML (125MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	--	Approved Prior to Jan 1, 1982	BRISTOL MYERS SQUIBB	Discontinued
DELALUTIN	016911	002	NDA	HYDROXYPROGESTERONE CAPROATE	SOLUTION;INTRAMUSCULAR	250MG/ML (250MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	--	Approved Prior to Jan 1, 1982	BRISTOL MYERS SQUIBB	Discontinued