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
82804-080-60	82804-080	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240305	N/A	ANDA	ANDA210015	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-080-60)
50090-7113-1	50090-7113	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240311	N/A	ANDA	ANDA210015	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7113-1)
50090-7113-2	50090-7113	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240311	N/A	ANDA	ANDA210015	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7113-2)
72189-539-30	72189-539	HUMAN PRESCRIPTION DRUG	Bupropion HCL ER (XL)	Bupropion HCL ER (XL)	TABLET, EXTENDED RELEASE	ORAL	20240301	N/A	ANDA	ANDA210015	Direct_RX	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-539-30)
72189-539-90	72189-539	HUMAN PRESCRIPTION DRUG	Bupropion HCL ER (XL)	Bupropion HCL ER (XL)	TABLET, EXTENDED RELEASE	ORAL	20240301	N/A	ANDA	ANDA210015	Direct_RX	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-539-90)
70436-011-02	70436-011	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20181201	N/A	ANDA	ANDA210015	Slate Run Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70436-011-02)
70436-011-04	70436-011	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20181201	N/A	ANDA	ANDA210015	Slate Run Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70436-011-04)
70436-011-06	70436-011	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20181201	N/A	ANDA	ANDA210015	Slate Run Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70436-011-06)
50090-7112-0	50090-7112	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240311	N/A	ANDA	ANDA210015	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-7112-0)
72789-377-90	72789-377	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240130	N/A	ANDA	ANDA210015	PD-Rx Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-377-90)
82804-080-90	82804-080	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240305	N/A	ANDA	ANDA210015	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-080-90)
70518-4014-0	70518-4014	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240207	N/A	ANDA	ANDA210015	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4014-0)
70518-4014-1	70518-4014	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250703	N/A	ANDA	ANDA210015	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4014-1)
50090-6961-0	50090-6961	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20231219	N/A	ANDA	ANDA210015	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6961-0)
50090-6961-1	50090-6961	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20231219	N/A	ANDA	ANDA210015	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6961-1)
50090-6962-0	50090-6962	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20231219	N/A	ANDA	ANDA210015	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6962-0)