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
16714-038-01	16714-038	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20201021	20240831	ANDA	ANDA091272	NorthStar RxLLC	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-038-01)
16714-905-01	16714-905	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190410	20240831	ANDA	ANDA091272	NorthStar RxLLC	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-905-01)
47335-758-81	47335-758	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20141215	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-81)
47335-758-88	47335-758	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20141215	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-88)
47335-758-99	47335-758	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190329	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	2 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-758-99) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
47335-759-08	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 (47335-759-08)
47335-758-18	47335-758	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20141215	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-18)
47335-758-08	47335-758	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20141215	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-08)
47335-758-83	47335-758	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20141215	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-83)
47335-759-18	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	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-759-18)
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)
47335-760-08	47335-760	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20141215	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-08)
47335-760-18	47335-760	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20141215	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-18)
47335-760-61	47335-760	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190329	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	10 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-760-61) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
47335-760-81	47335-760	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20141215	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-81)
47335-760-83	47335-760	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20141215	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-83)
47335-760-88	47335-760	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20141215	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-88)
47335-794-08	47335-794	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190215	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-08)
47335-794-13	47335-794	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190215	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-13)
47335-794-81	47335-794	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190815	N/A	ANDA	ANDA091272	Sun Pharmaceutical Industries, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-81)