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
70518-4116-0	70518-4116	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20240627	N/A	ANDA	ANDA214609	REMEDYREPACK INC.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4116-0)
43598-943-30	43598-943	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20210920	N/A	ANDA	ANDA214609	Dr. Reddy's Laboratories Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-943-30)
43598-943-90	43598-943	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20210920	N/A	ANDA	ANDA214609	Dr. Reddy's Laboratories Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-943-90)
43598-944-30	43598-944	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20210920	N/A	ANDA	ANDA214609	Dr. Reddy's Laboratories Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-944-30)
43598-944-90	43598-944	HUMAN PRESCRIPTION DRUG	Venlafaxine	Venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20210920	N/A	ANDA	ANDA214609	Dr. Reddy's Laboratories Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-944-90)