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
63187-713-30	63187-713	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160601	N/A	ANDA	ANDA077415	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-713-30)
63187-713-60	63187-713	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160601	N/A	ANDA	ANDA077415	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-713-60)
63187-713-90	63187-713	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160601	N/A	ANDA	ANDA077415	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-713-90)
0115-6811-02	0115-6811	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20090501	N/A	ANDA	ANDA077415	Amneal Pharmaceuticals of New York LLC	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6811-02)
0115-6811-08	0115-6811	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20090501	N/A	ANDA	ANDA077415	Amneal Pharmaceuticals of New York LLC	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6811-08)
0115-6811-10	0115-6811	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20090501	N/A	ANDA	ANDA077415	Amneal Pharmaceuticals of New York LLC	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6811-10)
45865-632-30	45865-632	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20150911	N/A	ANDA	ANDA077415	Medsource Pharmaceuticals	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45865-632-30)
45865-632-60	45865-632	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	BUPROPION HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20150911	N/A	ANDA	ANDA077415	Medsource Pharmaceuticals	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45865-632-60)