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
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	078466	007	ANDA	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	CAPSULE; ORAL	10MG; 40MG	No	No	2010/02/05	--	LUPIN PHARMS	Prescription
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	078466	007	ANDA	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	CAPSULE; ORAL	10MG; 40MG	No	No	2011/07/05	--	LUPIN PHARMS	Prescription
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	078652	001	ANDA	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	CAPSULE; ORAL	2.5MG; 10MG	No	No	2013/03/28 (TA)	--	ZYDUS PHARMS USA INC	None (Tentative Approval)
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	078652	002	ANDA	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	CAPSULE; ORAL	5MG; 10MG	No	No	2013/03/28 (TA)	--	ZYDUS PHARMS USA INC	None (Tentative Approval)
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	078652	003	ANDA	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	CAPSULE; ORAL	5MG; 20MG	No	No	2013/03/28 (TA)	--	ZYDUS PHARMS USA INC	None (Tentative Approval)
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	078652	004	ANDA	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	CAPSULE; ORAL	10MG; 20MG	No	No	2013/03/28 (TA)	--	ZYDUS PHARMS USA INC	None (Tentative Approval)