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
0527-2606-32	0527-2606	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20210406	N/A	ANDA	ANDA213927	Lannett Company, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BOTTLE (0527-2606-32)
0527-2606-46	0527-2606	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20210406	N/A	ANDA	ANDA213927	Lannett Company, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET in 1 BOTTLE (0527-2606-46)
0527-2616-32	0527-2616	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20221231	N/A	ANDA	ANDA213927	Lannett Company, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BOTTLE (0527-2616-32)
0527-2616-46	0527-2616	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET	ORAL	20221231	N/A	ANDA	ANDA213927	Lannett Company, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET in 1 BOTTLE (0527-2616-46)
42799-961-01	42799-961	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20230201	N/A	ANDA	ANDA213927	Edenbridge Pharmaceuticals LLC.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (42799-961-01)
42799-961-02	42799-961	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20230201	N/A	ANDA	ANDA213927	Edenbridge Pharmaceuticals LLC.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (42799-961-02)