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
47335-759-61	47335-759	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190329	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	10 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-759-61) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
47335-759-81	47335-759	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20141215	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-759-81)
47335-759-83	47335-759	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20141215	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-759-83)
47335-759-88	47335-759	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20141215	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-759-88)