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
72241-077-04	72241-077	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, COATED	ORAL	20180816	N/A	ANDA	ANDA211323	Modavar Pharmaceuticals LLC	VENLAFAXINE HYDROCHLORIDE	225 mg/1	90 TABLET, COATED in 1 BOTTLE (72241-077-04)
72241-077-11	72241-077	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, COATED	ORAL	20180816	N/A	ANDA	ANDA211323	Modavar Pharmaceuticals LLC	VENLAFAXINE HYDROCHLORIDE	225 mg/1	1000 TABLET, COATED in 1 BOTTLE (72241-077-11)
72241-077-22	72241-077	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, COATED	ORAL	20180816	N/A	ANDA	ANDA211323	Modavar Pharmaceuticals LLC	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET, COATED in 1 BOTTLE (72241-077-22)
75834-219-00	75834-219	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20190906	N/A	ANDA	ANDA211323	Nivagen Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-219-00)
75834-219-30	75834-219	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20190906	N/A	ANDA	ANDA211323	Nivagen Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-219-30)
75834-218-90	75834-218	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20190906	N/A	ANDA	ANDA211323	Nivagen Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-218-90)
75834-219-90	75834-219	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20190906	N/A	ANDA	ANDA211323	Nivagen Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-219-90)