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
50090-5163-0	50090-5163	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200923	N/A	ANDA	ANDA210497	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5163-0)
50090-5163-1	50090-5163	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200923	N/A	ANDA	ANDA210497	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5163-1)
50090-5163-2	50090-5163	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200923	N/A	ANDA	ANDA210497	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5163-2)
55700-820-30	55700-820	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20191122	20260831	ANDA	ANDA210497	Quality Care Products, LLC	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-820-30)
55700-820-90	55700-820	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20201112	20260331	ANDA	ANDA210497	Quality Care Products, LLC	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-820-90)
70518-2458-0	70518-2458	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20191129	N/A	ANDA	ANDA210497	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2458-0)
70518-2458-6	70518-2458	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20240812	N/A	ANDA	ANDA210497	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2458-6)
50090-5245-0	50090-5245	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20201012	N/A	ANDA	ANDA210497	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5245-0)
50090-5245-1	50090-5245	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20201012	N/A	ANDA	ANDA210497	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5245-1)
68001-519-03	68001-519	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20211213	N/A	ANDA	ANDA210497	BluePoint Laboratories	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-519-03)
68001-519-04	68001-519	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20211213	N/A	ANDA	ANDA210497	BluePoint Laboratories	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-519-04)
68001-519-05	68001-519	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20211213	N/A	ANDA	ANDA210497	BluePoint Laboratories	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-519-05)
71335-1214-1	71335-1214	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20190503	N/A	ANDA	ANDA210497	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-1)
71335-1214-2	71335-1214	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20210422	N/A	ANDA	ANDA210497	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-2)
68788-7786-1	68788-7786	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20201021	N/A	ANDA	ANDA210497	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-1)
68788-7786-3	68788-7786	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20201021	N/A	ANDA	ANDA210497	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-3)
68788-7786-6	68788-7786	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20201021	N/A	ANDA	ANDA210497	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-6)
68788-7786-8	68788-7786	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20201021	N/A	ANDA	ANDA210497	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-8)
68788-7786-9	68788-7786	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20201021	N/A	ANDA	ANDA210497	Preferred Pharmaceuticals Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-9)
80425-0461-1	80425-0461	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20241218	N/A	ANDA	ANDA210497	Advanced Rx of Tennessee, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0461-1)