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
57237-175-90	57237-175	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Rising Pharma Holdings, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET in 1 BOTTLE (57237-175-90)
65862-408-01	65862-408	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	100 mg/1	100 TABLET in 1 BOTTLE (65862-408-01)
65862-408-10	65862-408	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	100 mg/1	10 BLISTER PACK in 1 CARTON (65862-408-10) / 10 TABLET in 1 BLISTER PACK
65862-407-90	65862-407	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET in 1 BOTTLE (65862-407-90)
65862-407-99	65862-407	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	1000 TABLET in 1 BOTTLE (65862-407-99)
70518-1385-3	70518-1385	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20231107	N/A	ANDA	ANDA090555	REMEDYREPACK INC.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (70518-1385-3)
65862-406-90	65862-406	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	90 TABLET in 1 BOTTLE (65862-406-90)
65862-406-99	65862-406	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	1000 TABLET in 1 BOTTLE (65862-406-99)
65862-408-20	65862-408	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	100 mg/1	20 TABLET in 1 BOTTLE (65862-408-20)
65862-408-66	65862-408	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	100 mg/1	6000 TABLET in 1 BOTTLE (65862-408-66)
65862-408-90	65862-408	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	100 mg/1	90 TABLET in 1 BOTTLE (65862-408-90)
65862-408-99	65862-408	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	100 mg/1	1000 TABLET in 1 BOTTLE (65862-408-99)