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
71335-0877-1	71335-0877	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20180907	N/A	ANDA	ANDA207389	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET in 1 BOTTLE (71335-0877-1)
71335-0877-2	71335-0877	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20180621	N/A	ANDA	ANDA207389	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET in 1 BOTTLE (71335-0877-2)
71335-0877-3	71335-0877	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20211227	N/A	ANDA	ANDA207389	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET in 1 BOTTLE (71335-0877-3)
71335-0877-4	71335-0877	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20180913	N/A	ANDA	ANDA207389	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET in 1 BOTTLE (71335-0877-4)
71335-0877-5	71335-0877	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20211227	N/A	ANDA	ANDA207389	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	120 TABLET in 1 BOTTLE (71335-0877-5)
71335-0877-6	71335-0877	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20211227	N/A	ANDA	ANDA207389	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	15 TABLET in 1 BOTTLE (71335-0877-6)
71335-0877-7	71335-0877	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20211227	N/A	ANDA	ANDA207389	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	21 TABLET in 1 BOTTLE (71335-0877-7)
69097-918-02	69097-918	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20180526	N/A	ANDA	ANDA207389	CIPLA USA INC.,	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET in 1 BOTTLE (69097-918-02)
69097-918-07	69097-918	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20180526	N/A	ANDA	ANDA207389	CIPLA USA INC.,	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET in 1 BOTTLE (69097-918-07)
69097-918-15	69097-918	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20180526	N/A	ANDA	ANDA207389	CIPLA USA INC.,	BUPROPION HYDROCHLORIDE	100 mg/1	1000 TABLET in 1 BOTTLE (69097-918-15)
69097-917-15	69097-917	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20180526	N/A	ANDA	ANDA207389	CIPLA USA INC.,	BUPROPION HYDROCHLORIDE	75 mg/1	1000 TABLET in 1 BOTTLE (69097-917-15)
69097-917-07	69097-917	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20180526	N/A	ANDA	ANDA207389	CIPLA USA INC.,	BUPROPION HYDROCHLORIDE	75 mg/1	100 TABLET in 1 BOTTLE (69097-917-07)
69097-917-02	69097-917	HUMAN PRESCRIPTION DRUG	bupropion Hydrochloride	bupropion Hydrochloride	TABLET	ORAL	20180526	N/A	ANDA	ANDA207389	CIPLA USA INC.,	BUPROPION HYDROCHLORIDE	75 mg/1	30 TABLET in 1 BOTTLE (69097-917-02)