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
29033-045-30	29033-045	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	venlafaxine hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20170327	N/A	ANDA	ANDA205468	Nostrum Laboratories, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (29033-045-30)
29033-045-90	29033-045	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	venlafaxine hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20170327	N/A	ANDA	ANDA205468	Nostrum Laboratories, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (29033-045-90)
69367-418-09	69367-418	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20251118	N/A	ANDA	ANDA205468	Westminster Pharmaceuticals, LLC	VENLAFAXINE HYDROCHLORIDE	225 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-418-09)
69367-418-30	69367-418	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20251118	N/A	ANDA	ANDA205468	Westminster Pharmaceuticals, LLC	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-418-30)
69367-417-09	69367-417	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20251118	N/A	ANDA	ANDA205468	Westminster Pharmaceuticals, LLC	VENLAFAXINE HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-417-09)
69367-417-30	69367-417	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20251118	N/A	ANDA	ANDA205468	Westminster Pharmaceuticals, LLC	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-417-30)
29033-046-30	29033-046	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	venlafaxine hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20170327	N/A	ANDA	ANDA205468	Nostrum Laboratories, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (29033-046-30)
29033-046-90	29033-046	HUMAN PRESCRIPTION DRUG	Venlafaxine Hydrochloride	venlafaxine hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20170327	N/A	ANDA	ANDA205468	Nostrum Laboratories, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (29033-046-90)