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
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)
68180-320-02	68180-320	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20170614	N/A	ANDA	ANDA090693	Lupin Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-320-02)
68180-320-06	68180-320	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20170614	N/A	ANDA	ANDA090693	Lupin Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-320-06)
68180-320-09	68180-320	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20170614	N/A	ANDA	ANDA090693	Lupin Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-320-09)
70518-4446-0	70518-4446	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250818	N/A	ANDA	ANDA090693	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4446-0)
82009-051-05	82009-051	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	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)
70518-2022-2	70518-2022	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250706	N/A	ANDA	ANDA090693	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2022-2)
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)