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
0591-3331-05	0591-3331	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20081126	N/A	ANDA	ANDA077715	Actavis Pharma, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-3331-05)
0591-3331-19	0591-3331	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20081126	N/A	ANDA	ANDA077715	Actavis Pharma, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-3331-19)
0591-3331-30	0591-3331	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20081126	N/A	ANDA	ANDA077715	Actavis Pharma, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-3331-30)
50090-4049-0	50090-4049	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190111	N/A	ANDA	ANDA077715	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4049-0)
50090-4049-1	50090-4049	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190111	N/A	ANDA	ANDA077715	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4049-1)
50090-4049-2	50090-4049	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190111	N/A	ANDA	ANDA077715	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4049-2)
53002-1495-0	53002-1495	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181001	N/A	ANDA	ANDA077715	RPK Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-1495-0)
53002-1495-3	53002-1495	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181001	N/A	ANDA	ANDA077715	RPK Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-1495-3)
63187-766-30	63187-766	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20161101	N/A	ANDA	ANDA077715	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-766-30)
63187-766-60	63187-766	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20161101	N/A	ANDA	ANDA077715	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-766-60)
63187-766-90	63187-766	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20161101	N/A	ANDA	ANDA077715	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-766-90)