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
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)
50090-4853-0	50090-4853	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20200120	N/A	ANDA	ANDA090555	A-S Medication Solutions	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET in 1 BOTTLE (50090-4853-0)
50090-4853-1	50090-4853	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20200120	N/A	ANDA	ANDA090555	A-S Medication Solutions	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 TABLET in 1 BOTTLE (50090-4853-1)
65862-406-01	65862-406	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	100 TABLET in 1 BOTTLE (65862-406-01)
65862-406-10	65862-406	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	10 BLISTER PACK in 1 CARTON (65862-406-10) / 10 TABLET in 1 BLISTER PACK
65862-406-30	65862-406	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	30 TABLET in 1 BOTTLE (65862-406-30)
65862-406-59	65862-406	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	5000 TABLET in 1 BOTTLE (65862-406-59)
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)
70518-1385-0	70518-1385	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20180824	N/A	ANDA	ANDA090555	REMEDYREPACK INC.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET in 1 BLISTER PACK (70518-1385-0)
70518-1385-1	70518-1385	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20181004	N/A	ANDA	ANDA090555	REMEDYREPACK INC.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-1385-1)
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)
51655-223-26	51655-223	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20230227	N/A	ANDA	ANDA090555	Northwind Health Company, LLC	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (51655-223-26)
51655-223-52	51655-223	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20221025	N/A	ANDA	ANDA090555	Northwind Health Company, LLC	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-223-52)
65862-407-01	65862-407	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	100 TABLET in 1 BOTTLE (65862-407-01)
65862-407-10	65862-407	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	10 BLISTER PACK in 1 CARTON (65862-407-10) / 10 TABLET in 1 BLISTER PACK
65862-407-30	65862-407	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BOTTLE (65862-407-30)
65862-407-71	65862-407	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	7000 TABLET in 1 BOTTLE (65862-407-71)
71335-1104-1	71335-1104	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20190220	N/A	ANDA	ANDA090555	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	60 TABLET in 1 BOTTLE (71335-1104-1)
71335-1104-2	71335-1104	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20190213	N/A	ANDA	ANDA090555	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BOTTLE (71335-1104-2)