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
50090-7349-0	50090-7349	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241016	N/A	ANDA	ANDA216800	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7349-0)
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)
50090-7423-0	50090-7423	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 (50090-7423-0)
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)
50090-7422-0	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)
50090-7422-3	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)
0615-8601-39	0615-8601	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20251031	N/A	ANDA	ANDA216800	NCS HealthCare of KY, LLC dba Vangard Labs	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8601-39)
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)
70518-4081-4	70518-4081	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250827	N/A	ANDA	ANDA216800	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4081-4)
70518-4093-0	70518-4093	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240604	N/A	ANDA	ANDA216800	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4093-0)
70518-4081-3	70518-4081	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250701	N/A	ANDA	ANDA216800	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4081-3)
70518-4081-1	70518-4081	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240926	N/A	ANDA	ANDA216800	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4081-1)
70518-4081-2	70518-4081	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250701	N/A	ANDA	ANDA216800	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4081-2)
71335-2400-2	71335-2400	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240613	N/A	ANDA	ANDA216800	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	200 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2400-2)
71335-2400-5	71335-2400	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240613	N/A	ANDA	ANDA216800	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	200 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2400-5)
71335-2400-6	71335-2400	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240613	N/A	ANDA	ANDA216800	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	200 mg/1	28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2400-6)
71335-2400-1	71335-2400	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240613	N/A	ANDA	ANDA216800	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	200 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2400-1)
71335-2400-3	71335-2400	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240613	N/A	ANDA	ANDA216800	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	200 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2400-3)
71335-2400-4	71335-2400	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240613	N/A	ANDA	ANDA216800	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	200 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2400-4)
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)