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
67046-1572-3	67046-1572	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250702	N/A	ANDA	ANDA216800	Coupler LLC	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1572-3)
68788-8769-1	68788-8769	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241119	N/A	ANDA	ANDA216800	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-1)
68788-8769-2	68788-8769	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241119	N/A	ANDA	ANDA216800	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	20 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-2)
68788-8769-3	68788-8769	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241119	N/A	ANDA	ANDA216800	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-3)
68788-8769-6	68788-8769	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241119	N/A	ANDA	ANDA216800	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-6)
68788-8769-8	68788-8769	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241119	N/A	ANDA	ANDA216800	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-8)
68788-8769-9	68788-8769	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241119	N/A	ANDA	ANDA216800	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-9)
0615-8602-39	0615-8602	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20251104	N/A	ANDA	ANDA216800	NCS HealthCare of KY, LLC dba Vangard Labs	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8602-39)
71335-2457-1	71335-2457	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240820	N/A	ANDA	ANDA216800	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-1)
71335-2457-2	71335-2457	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240820	N/A	ANDA	ANDA216800	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-2)
71335-2457-3	71335-2457	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240820	N/A	ANDA	ANDA216800	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-3)
71335-2457-4	71335-2457	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240820	N/A	ANDA	ANDA216800	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-4)
71335-2457-5	71335-2457	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240820	N/A	ANDA	ANDA216800	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-5)
71335-2457-6	71335-2457	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240820	N/A	ANDA	ANDA216800	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-6)
50090-7422-0	50090-7422	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241028	N/A	ANDA	ANDA216800	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7422-0)
50090-7422-1	50090-7422	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241028	N/A	ANDA	ANDA216800	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7422-1)
50090-7422-2	50090-7422	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241028	N/A	ANDA	ANDA216800	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7422-2)
50090-7422-3	50090-7422	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241028	N/A	ANDA	ANDA216800	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7422-3)
71335-2649-1	71335-2649	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250603	N/A	ANDA	ANDA216800	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-1)
71335-2649-2	71335-2649	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250603	N/A	ANDA	ANDA216800	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-2)