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
0615-8582-39	0615-8582	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20250718	N/A	ANDA	ANDA075491	NCS HealthCare of KY, LLC dba Vangard Labs	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8582-39)
50090-7511-0	50090-7511	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20250220	N/A	ANDA	ANDA075491	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-7511-0)
50090-7511-3	50090-7511	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20250220	N/A	ANDA	ANDA075491	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7511-3)
0615-8581-39	0615-8581	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20250718	N/A	ANDA	ANDA075491	NCS HealthCare of KY, LLC dba Vangard Labs	BUPROPION HYDROCHLORIDE	75 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8581-39)
59651-875-01	59651-875	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20240425	N/A	ANDA	ANDA075491	Aurobindo Pharma Limited	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-875-01)
59651-874-01	59651-874	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20240425	N/A	ANDA	ANDA075491	Aurobindo Pharma Limited	BUPROPION HYDROCHLORIDE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-874-01)
71335-2652-1	71335-2652	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20250603	N/A	ANDA	ANDA075491	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2652-1)
71335-2652-2	71335-2652	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20250603	N/A	ANDA	ANDA075491	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2652-2)
71335-2652-3	71335-2652	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20250603	N/A	ANDA	ANDA075491	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2652-3)
71335-2652-4	71335-2652	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20250603	N/A	ANDA	ANDA075491	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2652-4)
71335-2652-5	71335-2652	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20250603	N/A	ANDA	ANDA075491	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-2652-5)
71335-2652-6	71335-2652	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20250603	N/A	ANDA	ANDA075491	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-2652-6)
71335-2652-7	71335-2652	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20250603	N/A	ANDA	ANDA075491	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (71335-2652-7)