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
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)
68788-8677-6	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)
68788-8677-8	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)
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)
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)
50090-4747-0	50090-4747	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20191122	N/A	ANDA	ANDA090693	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4747-0)
50090-4747-1	50090-4747	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20191122	N/A	ANDA	ANDA090693	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4747-1)
50090-4747-2	50090-4747	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20191122	N/A	ANDA	ANDA090693	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4747-2)
50090-4749-0	50090-4749	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20191122	N/A	ANDA	ANDA090693	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4749-0)
50090-4749-1	50090-4749	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20191122	N/A	ANDA	ANDA090693	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4749-1)
68071-3928-9	68071-3928	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20251208	N/A	ANDA	ANDA090693	NuCare Pharmaceuticals,Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3928-9)
68071-3932-3	68071-3932	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20251209	N/A	ANDA	ANDA090693	NuCare Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3932-3)