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
65841-780-05	65841-780	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20140215	N/A	ANDA	ANDA201567	Zydus Lifesciences Limited	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-780-05)
65841-780-06	65841-780	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20140215	N/A	ANDA	ANDA201567	Zydus Lifesciences Limited	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-780-06)
65841-780-10	65841-780	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20140215	N/A	ANDA	ANDA201567	Zydus Lifesciences Limited	BUPROPION HYDROCHLORIDE	300 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-780-10)
65841-780-16	65841-780	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20140215	N/A	ANDA	ANDA201567	Zydus Lifesciences Limited	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-780-16)
65841-836-05	65841-836	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20180802	N/A	ANDA	ANDA201567	Zydus Lifesciences Limited	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-836-05)
65841-836-06	65841-836	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20180802	N/A	ANDA	ANDA201567	Zydus Lifesciences Limited	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-836-06)
65841-836-10	65841-836	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20180802	N/A	ANDA	ANDA201567	Zydus Lifesciences Limited	BUPROPION HYDROCHLORIDE	150 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-836-10)
65841-836-16	65841-836	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20180802	N/A	ANDA	ANDA201567	Zydus Lifesciences Limited	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-836-16)
68382-353-05	68382-353	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20180802	N/A	ANDA	ANDA201567	Zydus Pharmaceuticals USA Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-353-05)
68382-353-06	68382-353	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20180802	N/A	ANDA	ANDA201567	Zydus Pharmaceuticals USA Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-353-06)
68382-353-10	68382-353	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20180802	N/A	ANDA	ANDA201567	Zydus Pharmaceuticals USA Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-353-10)
68382-353-16	68382-353	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20180802	N/A	ANDA	ANDA201567	Zydus Pharmaceuticals USA Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-353-16)
68382-354-05	68382-354	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20140215	N/A	ANDA	ANDA201567	Zydus Pharmaceuticals USA Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-354-05)
68382-354-06	68382-354	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20140215	N/A	ANDA	ANDA201567	Zydus Pharmaceuticals USA Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-354-06)
68382-354-10	68382-354	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20140215	N/A	ANDA	ANDA201567	Zydus Pharmaceuticals USA Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-354-10)
68382-354-16	68382-354	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20140215	N/A	ANDA	ANDA201567	Zydus Pharmaceuticals USA Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-354-16)
63187-521-30	63187-521	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20181201	N/A	ANDA	ANDA201567	Proficient Rx LP	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-521-30)
63187-521-60	63187-521	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20181201	N/A	ANDA	ANDA201567	Proficient Rx LP	BUPROPION HYDROCHLORIDE	300 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-521-60)
63187-521-90	63187-521	HUMAN PRESCRIPTION DRUG	bupropion	bupropion	TABLET, EXTENDED RELEASE	ORAL	20181201	N/A	ANDA	ANDA201567	Proficient Rx LP	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-521-90)