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
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)
82009-052-05	82009-052	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	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)
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)
68180-319-02	68180-319	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20170614	N/A	ANDA	ANDA090693	Lupin Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-319-02)
68180-319-09	68180-319	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20170614	N/A	ANDA	ANDA090693	Lupin Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-319-09)
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)
68180-319-06	68180-319	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride XL	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)
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)
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)