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
71335-1114-4	71335-1114	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190329	N/A	ANDA	ANDA210081	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1114-4)
71335-1114-5	71335-1114	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240905	N/A	ANDA	ANDA210081	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	8 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1114-5)
71335-1114-6	71335-1114	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240905	N/A	ANDA	ANDA210081	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1114-6)
71335-1114-3	71335-1114	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190221	N/A	ANDA	ANDA210081	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1114-3)
71335-1114-1	71335-1114	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190222	N/A	ANDA	ANDA210081	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1114-1)
71335-1114-2	71335-1114	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240905	N/A	ANDA	ANDA210081	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1114-2)
24979-102-02	24979-102	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180830	N/A	ANDA	ANDA210081	TWi Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-102-02)
24979-102-06	24979-102	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180830	N/A	ANDA	ANDA210081	TWi Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-102-06)
24979-102-07	24979-102	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180830	N/A	ANDA	ANDA210081	TWi Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-102-07)
24979-101-06	24979-101	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180830	N/A	ANDA	ANDA210081	TWi Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-101-06)
24979-101-02	24979-101	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180830	N/A	ANDA	ANDA210081	TWi Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-101-02)
24979-101-07	24979-101	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180830	N/A	ANDA	ANDA210081	TWi Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-101-07)