美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
65862-405-30	65862-405	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET in 1 BOTTLE (65862-405-30)
65862-405-60	65862-405	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	60 TABLET in 1 BOTTLE (65862-405-60)
65862-405-66	65862-405	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	6000 TABLET in 1 BOTTLE (65862-405-66)
65862-405-90	65862-405	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 TABLET in 1 BOTTLE (65862-405-90)
65862-405-99	65862-405	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	1000 TABLET in 1 BOTTLE (65862-405-99)
60760-304-30	60760-304	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20200616	N/A	ANDA	ANDA090555	St. Mary's Medical Park Pharmacy	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (60760-304-30)
60760-187-60	60760-187	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20190529	N/A	ANDA	ANDA090555	St. Mary's Medical Park Pharmacy	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (60760-187-60)
70518-2659-0	70518-2659	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20200327	N/A	ANDA	ANDA090555	REMEDYREPACK INC.	VENLAFAXINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BLISTER PACK (70518-2659-0)