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
83301-0025-3	83301-0025	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240617	N/A	ANDA	ANDA208652	Mullan Phamaceutical Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (83301-0025-3)
83301-0025-4	83301-0025	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240617	N/A	ANDA	ANDA208652	Mullan Phamaceutical Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (83301-0025-4)
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)