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
69367-288-05	69367-288	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180529	N/A	ANDA	ANDA207224	Westminster Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-288-05)
69367-288-09	69367-288	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20171001	N/A	ANDA	ANDA207224	Westminster Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-288-09)
69367-289-05	69367-289	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20171001	N/A	ANDA	ANDA207224	Westminster Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-289-05)
69367-289-09	69367-289	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20171001	N/A	ANDA	ANDA207224	Westminster Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-289-09)
71205-291-30	71205-291	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190701	N/A	ANDA	ANDA207224	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-291-30)
71205-291-60	71205-291	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190701	N/A	ANDA	ANDA207224	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-291-60)
71205-291-90	71205-291	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190701	N/A	ANDA	ANDA207224	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-291-90)
80425-0468-1	80425-0468	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250101	N/A	ANDA	ANDA207224	Advanced Rx of Tennessee, LLC	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0468-1)
80425-0468-2	80425-0468	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250101	N/A	ANDA	ANDA207224	Advanced Rx of Tennessee, LLC	BUPROPION HYDROCHLORIDE	300 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0468-2)
80425-0468-3	80425-0468	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250101	N/A	ANDA	ANDA207224	Advanced Rx of Tennessee, LLC	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0468-3)
42806-348-05	42806-348	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180529	N/A	ANDA	ANDA207224	Epic Pharma, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-348-05)
42806-348-09	42806-348	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20171001	N/A	ANDA	ANDA207224	Epic Pharma, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-348-09)
42806-348-30	42806-348	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20171001	N/A	ANDA	ANDA207224	Epic Pharma, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-348-30)
42806-349-05	42806-349	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20171001	N/A	ANDA	ANDA207224	Epic Pharma, LLC	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-349-05)
42806-349-09	42806-349	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20171001	N/A	ANDA	ANDA207224	Epic Pharma, LLC	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-349-09)