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
71335-9704-3	71335-9704	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20231010	N/A	ANDA	ANDA077653	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 TABLET in 1 BOTTLE (71335-9704-3)
71335-9704-4	71335-9704	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20240405	N/A	ANDA	ANDA077653	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	10 TABLET in 1 BOTTLE (71335-9704-4)
68382-019-01	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	100 TABLET in 1 BOTTLE (68382-019-01)
68382-019-05	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	500 TABLET in 1 BOTTLE (68382-019-05)
68382-019-06	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET in 1 BOTTLE (68382-019-06)
68382-019-10	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	1000 TABLET in 1 BOTTLE (68382-019-10)
68382-019-14	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	60 TABLET in 1 BOTTLE (68382-019-14)
68382-019-16	68382-019	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 TABLET in 1 BOTTLE (68382-019-16)
67046-1124-3	67046-1124	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20241111	N/A	ANDA	ANDA077653	Coupler LLC	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET in 1 BLISTER PACK (67046-1124-3)
68001-158-00	68001-158	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20131125	N/A	ANDA	ANDA077653	BluePoint Laboratories	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	100 TABLET in 1 BOTTLE (68001-158-00)