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
55154-3371-0	55154-3371	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20110601	N/A	ANDA	ANDA090174	Cardinal Health 107, LLC	VENLAFAXINE HYDROCHLORIDE	75 mg/1	10 BLISTER PACK in 1 BAG (55154-3371-0) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
61919-222-60	61919-222	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	CAPSULE, EXTENDED RELEASE	ORAL	20140101	N/A	ANDA	ANDA090174	DIRECT RX	VENLAFAXINE HYDROCHLORIDE	75 mg/1	60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (61919-222-60)
61919-222-30	61919-222	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	CAPSULE, EXTENDED RELEASE	ORAL	20200812	N/A	ANDA	ANDA090174	DIRECT RX	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (61919-222-30)
65841-752-06	65841-752	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20110601	N/A	ANDA	ANDA090174	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-752-06)
65841-752-10	65841-752	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20110601	N/A	ANDA	ANDA090174	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-752-10)
65841-752-16	65841-752	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20110601	N/A	ANDA	ANDA090174	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-752-16)
65841-753-06	65841-753	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20110601	N/A	ANDA	ANDA090174	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-753-06)
65841-753-10	65841-753	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20110601	N/A	ANDA	ANDA090174	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	150 mg/1	1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-753-10)
65841-753-16	65841-753	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20110601	N/A	ANDA	ANDA090174	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	150 mg/1	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-753-16)
71335-1338-1	71335-1338	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220209	N/A	ANDA	ANDA090174	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1338-1)
71335-1338-2	71335-1338	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220209	N/A	ANDA	ANDA090174	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1338-2)
71335-1338-3	71335-1338	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220209	N/A	ANDA	ANDA090174	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1338-3)
71335-1338-4	71335-1338	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220209	N/A	ANDA	ANDA090174	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1338-4)
71335-1338-5	71335-1338	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220209	N/A	ANDA	ANDA090174	Bryant Ranch Prepack	VENLAFAXINE HYDROCHLORIDE	75 mg/1	7 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1338-5)
65841-751-06	65841-751	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20110601	N/A	ANDA	ANDA090174	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-751-06)
70518-0478-1	70518-0478	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20201125	N/A	ANDA	ANDA090174	REMEDYREPACK INC.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-0478-1)
70518-0558-0	70518-0558	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20170530	N/A	ANDA	ANDA090174	REMEDYREPACK INC.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-0558-0)
65841-751-16	65841-751	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20110601	N/A	ANDA	ANDA090174	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-751-16)
65841-751-10	65841-751	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20110601	N/A	ANDA	ANDA090174	Zydus Lifesciences Limited	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-751-10)
16714-044-01	16714-044	HUMAN PRESCRIPTION DRUG	venlafaxine hydrochloride	venlafaxine hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20210610	20240731	ANDA	ANDA090174	Northstar Rx LLC.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16714-044-01)