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
71335-2709-3	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)
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)
68001-159-00	68001-159	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20131125	N/A	ANDA	ANDA077653	BluePoint Laboratories	VENLAFAXINE HYDROCHLORIDE	50 mg/1	100 TABLET in 1 BOTTLE (68001-159-00)
65841-673-01	65841-673	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	100 TABLET in 1 BOTTLE (65841-673-01)
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)
68071-3431-0	68071-3431	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20230727	N/A	ANDA	ANDA077653	NuCare Pharmaceuticals,Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	100 TABLET in 1 BOTTLE (68071-3431-0)
68084-896-25	68084-896	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20150929	N/A	ANDA	ANDA077653	American Health Packaging	VENLAFAXINE HYDROCHLORIDE	25 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-896-25) / 1 TABLET in 1 BLISTER PACK (68084-896-95)
68001-156-00	68001-156	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20131125	N/A	ANDA	ANDA077653	BluePoint Laboratories	VENLAFAXINE HYDROCHLORIDE	100 mg/1	100 TABLET in 1 BOTTLE (68001-156-00)
68001-160-00	68001-160	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20131125	N/A	ANDA	ANDA077653	BluePoint Laboratories	VENLAFAXINE HYDROCHLORIDE	75 mg/1	100 TABLET in 1 BOTTLE (68001-160-00)
63187-414-30	63187-414	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20190101	N/A	ANDA	ANDA077653	Proficient Rx LP	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BOTTLE (63187-414-30)
63187-414-60	63187-414	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20190101	N/A	ANDA	ANDA077653	Proficient Rx LP	VENLAFAXINE HYDROCHLORIDE	75 mg/1	60 TABLET in 1 BOTTLE (63187-414-60)
65841-674-01	65841-674	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	100 TABLET in 1 BOTTLE (65841-674-01)
65841-674-05	65841-674	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	500 TABLET in 1 BOTTLE (65841-674-05)
65841-674-06	65841-674	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BOTTLE (65841-674-06)
65841-674-10	65841-674	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	1000 TABLET in 1 BOTTLE (65841-674-10)
65841-674-14	65841-674	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET	ORAL	20080613	N/A	ANDA	ANDA077653	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	60 TABLET in 1 BOTTLE (65841-674-14)
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)