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
71335-0135-5	71335-0135	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241008	N/A	ANDA	ANDA079095	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	45 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-5)
71335-0135-6	71335-0135	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241008	N/A	ANDA	ANDA079095	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-6)
71335-0135-7	71335-0135	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241008	N/A	ANDA	ANDA079095	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-7)
71335-0135-8	71335-0135	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241008	N/A	ANDA	ANDA079095	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	56 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-8)
71335-0135-9	71335-0135	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241008	N/A	ANDA	ANDA079095	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-9)
71335-0135-3	71335-0135	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190911	N/A	ANDA	ANDA079095	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-3)
71335-0135-4	71335-0135	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241008	N/A	ANDA	ANDA079095	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-4)
71335-0135-1	71335-0135	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride SR	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190911	N/A	ANDA	ANDA079095	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-1)