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
0008-0836-21	0008-0836	HUMAN PRESCRIPTION DRUG	Effexor XR	VENLAFAXINE HYDROCHLORIDE	CAPSULE, EXTENDED RELEASE	ORAL	19971101	20260630	NDA	NDA020699	Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0008-0836-21)
58151-126-93	58151-126	HUMAN PRESCRIPTION DRUG	Effexor XR	VENLAFAXINE HYDROCHLORIDE	CAPSULE, EXTENDED RELEASE	ORAL	20241030	N/A	NDA	NDA020699	Viatris Specialty LLC	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-126-93)
58151-126-77	58151-126	HUMAN PRESCRIPTION DRUG	Effexor XR	VENLAFAXINE HYDROCHLORIDE	CAPSULE, EXTENDED RELEASE	ORAL	20241030	N/A	NDA	NDA020699	Viatris Specialty LLC	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-126-77)
58151-125-93	58151-125	HUMAN PRESCRIPTION DRUG	Effexor XR	VENLAFAXINE HYDROCHLORIDE	CAPSULE, EXTENDED RELEASE	ORAL	20240717	N/A	NDA	NDA020699	Viatris Specialty LLC	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-125-93)
58151-125-77	58151-125	HUMAN PRESCRIPTION DRUG	Effexor XR	VENLAFAXINE HYDROCHLORIDE	CAPSULE, EXTENDED RELEASE	ORAL	20240717	N/A	NDA	NDA020699	Viatris Specialty LLC	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-125-77)
58151-127-93	58151-127	HUMAN PRESCRIPTION DRUG	Effexor XR	VENLAFAXINE HYDROCHLORIDE	CAPSULE, EXTENDED RELEASE	ORAL	20250701	N/A	NDA	NDA020699	Viatris Specialty LLC	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-127-93)
58151-127-77	58151-127	HUMAN PRESCRIPTION DRUG	Effexor XR	VENLAFAXINE HYDROCHLORIDE	CAPSULE, EXTENDED RELEASE	ORAL	20240801	N/A	NDA	NDA020699	Viatris Specialty LLC	VENLAFAXINE HYDROCHLORIDE	150 mg/1	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-127-77)