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
0904-7505-61	0904-7505	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241125	N/A	ANDA	ANDA090693	Major Pharmaceuticals	BUPROPION HYDROCHLORIDE	150 mg/1	100 BLISTER PACK in 1 CARTON (0904-7505-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0904-7505-04	0904-7505	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241125	N/A	ANDA	ANDA090693	Major Pharmaceuticals	BUPROPION HYDROCHLORIDE	150 mg/1	30 BLISTER PACK in 1 CARTON (0904-7505-04) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0904-7469-04	0904-7469	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241007	N/A	ANDA	ANDA090693	Major Pharmaceuticals	BUPROPION HYDROCHLORIDE	300 mg/1	30 BLISTER PACK in 1 CARTON (0904-7469-04) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
82009-051-05	82009-051	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230707	N/A	ANDA	ANDA090693	Quallent Pharmaceuticals Health LLC	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (82009-051-05)
82009-052-05	82009-052	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230707	N/A	ANDA	ANDA090693	Quallent Pharmaceuticals Health LLC	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (82009-052-05)
61919-558-72	61919-558	HUMAN PRESCRIPTION DRUG	Bupropion HCL ER (XL)	Bupropion HCL ER (XL)	TABLET, EXTENDED RELEASE	ORAL	20240215	N/A	ANDA	ANDA090693	Direct_Rx	BUPROPION HYDROCHLORIDE	150 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-558-72)
50090-6789-0	50090-6789	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20231031	N/A	ANDA	ANDA090693	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6789-0)
68071-3559-9	68071-3559	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240109	N/A	ANDA	ANDA090693	NuCare Pharmaceuticals,Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3559-9)
68788-8677-6	68788-8677	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240523	N/A	ANDA	ANDA090693	Preferred Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8677-6)
68788-8677-9	68788-8677	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240523	N/A	ANDA	ANDA090693	Preferred Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8677-9)
68788-8677-1	68788-8677	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240523	N/A	ANDA	ANDA090693	Preferred Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8677-1)
68788-8677-3	68788-8677	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240523	N/A	ANDA	ANDA090693	Preferred Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8677-3)
68788-8677-8	68788-8677	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240523	N/A	ANDA	ANDA090693	Preferred Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8677-8)
70518-0859-0	70518-0859	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20171120	N/A	ANDA	ANDA090693	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-0859-0)
60687-782-01	60687-782	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240115	N/A	ANDA	ANDA090693	American Health Packaging	BUPROPION HYDROCHLORIDE	150 mg/1	100 BLISTER PACK in 1 CARTON (60687-782-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-782-11)
60687-793-21	60687-793	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240115	N/A	ANDA	ANDA090693	American Health Packaging	BUPROPION HYDROCHLORIDE	300 mg/1	30 BLISTER PACK in 1 CARTON (60687-793-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-793-11)
51655-098-52	51655-098	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230407	N/A	ANDA	ANDA090693	Northwind Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-098-52)
51655-098-83	51655-098	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230103	N/A	ANDA	ANDA090693	Northwind Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-098-83)
51655-098-26	51655-098	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220906	N/A	ANDA	ANDA090693	Northwind Pharmaceuticals, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-098-26)
68180-319-06	68180-319	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20170614	N/A	ANDA	ANDA090693	Lupin Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-319-06)