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
71335-1213-1	71335-1213	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20220209	N/A	ANDA	ANDA090555	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET in 1 BOTTLE (71335-1213-1)
71335-1213-2	71335-1213	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20220209	N/A	ANDA	ANDA090555	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	60 TABLET in 1 BOTTLE (71335-1213-2)
71335-1213-3	71335-1213	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20220209	N/A	ANDA	ANDA090555	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 TABLET in 1 BOTTLE (71335-1213-3)
71335-1213-4	71335-1213	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20220209	N/A	ANDA	ANDA090555	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	10 TABLET in 1 BOTTLE (71335-1213-4)
57237-176-01	57237-176	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Rising Pharma Holdings, Inc.	VENLAFAXINE HYDROCHLORIDE	100 mg/1	100 TABLET in 1 BOTTLE (57237-176-01)
57237-176-90	57237-176	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Rising Pharma Holdings, Inc.	VENLAFAXINE HYDROCHLORIDE	100 mg/1	90 TABLET in 1 BOTTLE (57237-176-90)
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)
71335-1104-3	71335-1104	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20200103	N/A	ANDA	ANDA090555	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET in 1 BOTTLE (71335-1104-3)
70518-1976-0	70518-1976	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20190325	N/A	ANDA	ANDA090555	REMEDYREPACK INC.	VENLAFAXINE HYDROCHLORIDE	100 mg/1	30 TABLET in 1 BLISTER PACK (70518-1976-0)
57237-173-01	57237-173	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Rising Pharma Holdings, Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	100 TABLET in 1 BOTTLE (57237-173-01)
57237-173-90	57237-173	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Rising Pharma Holdings, Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 TABLET in 1 BOTTLE (57237-173-90)
70518-2652-0	70518-2652	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20200325	N/A	ANDA	ANDA090555	REMEDYREPACK INC.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-2652-0)
70518-2652-1	70518-2652	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20200327	N/A	ANDA	ANDA090555	REMEDYREPACK INC.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BLISTER PACK (70518-2652-1)
70518-2652-2	70518-2652	HUMAN PRESCRIPTION DRUG	venlafaxine	venlafaxine hydrochloride	TABLET	ORAL	20201223	N/A	ANDA	ANDA090555	REMEDYREPACK INC.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (70518-2652-2)
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)
65862-405-01	65862-405	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	100 TABLET in 1 BOTTLE (65862-405-01)
65862-405-10	65862-405	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine Hydrochloride	TABLET	ORAL	20100407	N/A	ANDA	ANDA090555	Aurobindo Pharma Limited	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	10 BLISTER PACK in 1 CARTON (65862-405-10) / 10 TABLET in 1 BLISTER PACK
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)