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
DAUNORUBICIN HYDROCHLORIDE	050731	001	NDA	DAUNORUBICIN HYDROCHLORIDE	INJECTABLE;INJECTION	EQ 5MG BASE/ML	Yes	Yes	1998/01/30	1998/01/30	HIKMA	Prescription
DAUNORUBICIN HYDROCHLORIDE	064212	001	ANDA	DAUNORUBICIN HYDROCHLORIDE	INJECTABLE;INJECTION	EQ 20MG BASE/VIAL	No	No	1998/06/23	1998/06/23	TEVA PARENTERAL	Discontinued
DAUNORUBICIN HYDROCHLORIDE	064212	002	ANDA	DAUNORUBICIN HYDROCHLORIDE	INJECTABLE;INJECTION	EQ 50MG BASE/VIAL	No	No	1998/06/23	1999/05/03	TEVA PARENTERAL	Discontinued
DAUNORUBICIN HYDROCHLORIDE	065000	001	ANDA	DAUNORUBICIN HYDROCHLORIDE	INJECTABLE;INJECTION	EQ 20MG BASE/VIAL	No	No	1999/05/25	1999/05/25	FRESENIUS KABI USA	Prescription
DAUNORUBICIN HYDROCHLORIDE	065035	001	ANDA	DAUNORUBICIN HYDROCHLORIDE	INJECTABLE;INJECTION	EQ 5MG BASE/ML	No	No	2000/01/24	2000/01/24	MEITHEAL	Prescription
DAUNORUBICIN HYDROCHLORIDE	065034	001	ANDA	DAUNORUBICIN HYDROCHLORIDE	INJECTABLE;INJECTION	EQ 5MG BASE/VIAL	No	No	2001/11/20	2001/11/20	FRESENIUS KABI USA	Prescription
DAUNORUBICIN HYDROCHLORIDE	208759	001	ANDA	DAUNORUBICIN HYDROCHLORIDE	INJECTABLE;INJECTION	EQ 5MG BASE/ML	No	No	2019/04/12	2019/04/12	HISUN PHARM HANGZHOU	Prescription
DAUNORUBICIN HYDROCHLORIDE	206195	001	ANDA	DAUNORUBICIN HYDROCHLORIDE	INJECTABLE;INJECTION	EQ 20MG BASE/VIAL	No	No	2019/04/25	2019/04/25	HISUN PHARM HANGZHOU	Discontinued