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
69097-875-02	69097-875	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160829	N/A	ANDA	ANDA206556	CIPLA USA INC.,	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-875-02)
69097-875-05	69097-875	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160829	N/A	ANDA	ANDA206556	CIPLA USA INC.,	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-875-05)
69097-875-12	69097-875	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160829	N/A	ANDA	ANDA206556	CIPLA USA INC.,	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-875-12)
69097-876-02	69097-876	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160829	N/A	ANDA	ANDA206556	CIPLA USA INC.,	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-876-02)
69097-876-12	69097-876	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160829	N/A	ANDA	ANDA206556	CIPLA USA INC.,	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-876-12)
82804-013-30	82804-013	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230921	N/A	ANDA	ANDA206556	Proficient Rx LP	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-013-30)
82804-013-60	82804-013	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230921	N/A	ANDA	ANDA206556	Proficient Rx LP	BUPROPION HYDROCHLORIDE	300 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-013-60)
82804-013-90	82804-013	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230921	N/A	ANDA	ANDA206556	Proficient Rx LP	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-013-90)
70518-3846-0	70518-3846	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230831	N/A	ANDA	ANDA206556	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3846-0)
70518-3846-1	70518-3846	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20231117	N/A	ANDA	ANDA206556	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3846-1)
76282-480-05	76282-480	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190201	N/A	ANDA	ANDA206556	Exelan Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-480-05)
76282-480-30	76282-480	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220210	N/A	ANDA	ANDA206556	Exelan Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-480-30)
76282-480-90	76282-480	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220210	N/A	ANDA	ANDA206556	Exelan Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-480-90)
76282-481-05	76282-481	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220210	N/A	ANDA	ANDA206556	Exelan Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-481-05)
76282-481-30	76282-481	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20170612	N/A	ANDA	ANDA206556	Exelan Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-481-30)
76282-481-90	76282-481	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220210	N/A	ANDA	ANDA206556	Exelan Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-481-90)
68788-8537-1	68788-8537	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20231019	N/A	ANDA	ANDA206556	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-8537-1)
68788-8537-3	68788-8537	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20231019	N/A	ANDA	ANDA206556	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-8537-3)
68788-8537-6	68788-8537	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20231019	N/A	ANDA	ANDA206556	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-8537-6)
68788-8537-8	68788-8537	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20231019	N/A	ANDA	ANDA206556	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-8537-8)