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
65841-673-05	65841-673	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	500 TABLET in 1 BOTTLE (65841-673-05)
65841-673-06	65841-673	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	30 TABLET in 1 BOTTLE (65841-673-06)
65841-673-10	65841-673	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	1000 TABLET in 1 BOTTLE (65841-673-10)
65841-673-14	65841-673	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	60 TABLET in 1 BOTTLE (65841-673-14)
65841-673-16	65841-673	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	90 TABLET in 1 BOTTLE (65841-673-16)
65841-675-10	65841-675	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	100 mg/1	1000 TABLET in 1 BOTTLE (65841-675-10)
65841-675-14	65841-675	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	100 mg/1	60 TABLET in 1 BOTTLE (65841-675-14)
65841-675-16	65841-675	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	100 mg/1	90 TABLET in 1 BOTTLE (65841-675-16)
71335-2709-1	71335-2709	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20250926	N/A	ANDA	ANDA077653	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	100 mg/1	30 TABLET in 1 BOTTLE (71335-2709-1)
71335-2709-2	71335-2709	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20250926	N/A	ANDA	ANDA077653	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	100 mg/1	60 TABLET in 1 BOTTLE (71335-2709-2)
71335-2709-3	71335-2709	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20250926	N/A	ANDA	ANDA077653	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	100 mg/1	90 TABLET in 1 BOTTLE (71335-2709-3)
71335-2709-4	71335-2709	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20250926	N/A	ANDA	ANDA077653	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	100 mg/1	18 TABLET in 1 BOTTLE (71335-2709-4)