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
68001-496-04	68001-496	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20210430	N/A	ANDA	ANDA214419	BluePoint Laboratories	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-496-04)
72865-197-30	72865-197	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20210226	N/A	ANDA	ANDA214419	XLCare Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-197-30)
72865-197-90	72865-197	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20210226	N/A	ANDA	ANDA214419	XLCare Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-197-90)
43602-394-05	43602-394	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20201023	N/A	ANDA	ANDA214419	Ascent Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43602-394-05)
43602-394-30	43602-394	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20201023	N/A	ANDA	ANDA214419	Ascent Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43602-394-30)
31722-126-30	31722-126	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20201023	N/A	ANDA	ANDA214419	Camber Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-126-30)
31722-126-90	31722-126	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20201023	N/A	ANDA	ANDA214419	Camber Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-126-90)
68001-497-04	68001-497	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20210430	N/A	ANDA	ANDA214419	BluePoint Laboratories	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-497-04)
72865-198-30	72865-198	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20210226	N/A	ANDA	ANDA214419	XLCare Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-198-30)
72865-198-90	72865-198	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20210226	N/A	ANDA	ANDA214419	XLCare Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-198-90)
43602-395-05	43602-395	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20201023	N/A	ANDA	ANDA214419	Ascent Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43602-395-05)
43602-395-30	43602-395	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20201023	N/A	ANDA	ANDA214419	Ascent Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43602-395-30)
31722-123-30	31722-123	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20201023	N/A	ANDA	ANDA214419	Camber Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-123-30)
31722-123-90	31722-123	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20201023	N/A	ANDA	ANDA214419	Camber Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-123-90)
68001-499-04	68001-499	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20210430	N/A	ANDA	ANDA214419	BluePoint Laboratories	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-499-04)
72865-200-30	72865-200	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20210226	N/A	ANDA	ANDA214419	XLCare Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-200-30)
72865-200-90	72865-200	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20210226	N/A	ANDA	ANDA214419	XLCare Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	225 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-200-90)
43602-393-05	43602-393	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20201023	N/A	ANDA	ANDA214419	Ascent Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43602-393-05)
43602-393-30	43602-393	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20201023	N/A	ANDA	ANDA214419	Ascent Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	75 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43602-393-30)
31722-125-30	31722-125	HUMAN PRESCRIPTION DRUG	VENLAFAXINE HYDROCHLORIDE	venlafaxine	TABLET, EXTENDED RELEASE	ORAL	20201023	N/A	ANDA	ANDA214419	Camber Pharmaceuticals, Inc.	VENLAFAXINE HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-125-30)