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
70710-1352-9	70710-1352	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20220901	N/A	ANDA	ANDA215622	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1352-9)
70710-1348-3	70710-1348	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20220901	N/A	ANDA	ANDA215622	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1348-3)
70710-1348-9	70710-1348	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20220901	N/A	ANDA	ANDA215622	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1348-9)
70710-1349-1	70710-1349	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20220901	N/A	ANDA	ANDA215622	Zydus Pharmaceuticals USA Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1349-1)