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
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)
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)
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)
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)
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)
61919-558-60	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	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-558-60)
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)
61919-558-90	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	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-558-90)