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
59651-846-01	59651-846	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250603	N/A	ANDA	ANDA090325	Aurobindo Pharma Limited	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-846-01)
59651-846-05	59651-846	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250603	N/A	ANDA	ANDA090325	Aurobindo Pharma Limited	BUPROPION HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-846-05)
59651-848-01	59651-848	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250603	N/A	ANDA	ANDA090325	Aurobindo Pharma Limited	BUPROPION HYDROCHLORIDE	200 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-848-01)
59651-848-60	59651-848	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250603	N/A	ANDA	ANDA090325	Aurobindo Pharma Limited	BUPROPION HYDROCHLORIDE	200 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-848-60)
59651-847-01	59651-847	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250603	N/A	ANDA	ANDA090325	Aurobindo Pharma Limited	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-847-01)
59651-847-05	59651-847	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250603	N/A	ANDA	ANDA090325	Aurobindo Pharma Limited	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-847-05)