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
13811-715-30	13811-715	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	venlafaxine hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20100429	20260930	NDA AUTHORIZED GENERIC	NDA022104	Trigen Laboratories, LLC	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-715-30)
80425-0477-1	80425-0477	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	venlafaxine hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250130	N/A	NDA AUTHORIZED GENERIC	NDA022104	Advanced Rx of Tennessee, LLC	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-1)
80425-0477-2	80425-0477	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	venlafaxine hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250130	N/A	NDA AUTHORIZED GENERIC	NDA022104	Advanced Rx of Tennessee, LLC	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-2)
80425-0477-3	80425-0477	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	venlafaxine hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250130	N/A	NDA AUTHORIZED GENERIC	NDA022104	Advanced Rx of Tennessee, LLC	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-3)
13811-712-30	13811-712	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	venlafaxine hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20100429	20261231	NDA AUTHORIZED GENERIC	NDA022104	Trigen Laboratories, LLC	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-712-30)
13811-712-90	13811-712	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	venlafaxine hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20100429	20261231	NDA AUTHORIZED GENERIC	NDA022104	Trigen Laboratories, LLC	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-712-90)