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
70710-1350-9	70710-1350	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20220901	N/A	ANDA	ANDA215622	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1350-9)
70771-1651-1	70771-1651	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20220901	N/A	ANDA	ANDA215622	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	150 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1651-1)
70771-1651-3	70771-1651	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20220901	N/A	ANDA	ANDA215622	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1651-3)
70771-1651-9	70771-1651	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20220901	N/A	ANDA	ANDA215622	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1651-9)