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
0527-2415-46	0527-2415	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220131	N/A	ANDA	ANDA208652	Lannett Company Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2415-46)
0527-2415-43	0527-2415	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220131	N/A	ANDA	ANDA208652	Lannett Company Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2415-43)
0527-2415-41	0527-2415	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220131	N/A	ANDA	ANDA208652	Lannett Company Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2415-41)
0527-2415-32	0527-2415	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220131	N/A	ANDA	ANDA208652	Lannett Company Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2415-32)
0527-2430-32	0527-2430	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220131	N/A	ANDA	ANDA208652	Lannett Company Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2430-32)
0527-2430-41	0527-2430	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220131	N/A	ANDA	ANDA208652	Lannett Company Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2430-41)
0527-2430-43	0527-2430	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220131	N/A	ANDA	ANDA208652	Lannett Company Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2430-43)
0527-2430-46	0527-2430	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220131	N/A	ANDA	ANDA208652	Lannett Company Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2430-46)
71335-0824-1	71335-0824	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180515	N/A	ANDA	ANDA208652	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0824-1)
71335-0824-5	71335-0824	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180515	N/A	ANDA	ANDA208652	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	8 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0824-5)
71335-0824-2	71335-0824	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180515	N/A	ANDA	ANDA208652	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0824-2)
71335-0824-3	71335-0824	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180515	N/A	ANDA	ANDA208652	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0824-3)
71335-0824-4	71335-0824	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180515	N/A	ANDA	ANDA208652	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0824-4)
71205-045-30	71205-045	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180601	N/A	ANDA	ANDA208652	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-045-30)
71205-045-60	71205-045	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180601	N/A	ANDA	ANDA208652	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-045-60)
71205-045-90	71205-045	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180601	N/A	ANDA	ANDA208652	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-045-90)
71205-248-60	71205-248	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190401	N/A	ANDA	ANDA208652	Proficient Rx LP	BUPROPION HYDROCHLORIDE	300 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-248-60)
71205-248-90	71205-248	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190401	N/A	ANDA	ANDA208652	Proficient Rx LP	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-248-90)
71205-248-30	71205-248	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190401	N/A	ANDA	ANDA208652	Proficient Rx LP	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-248-30)
71335-1542-2	71335-1542	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride (XL)	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200327	N/A	ANDA	ANDA208652	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1542-2)