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
42806-415-05	42806-415	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20211215	N/A	ANDA	ANDA075932	Epic Pharma LLC	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-415-05)
42806-415-52	42806-415	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20211215	N/A	ANDA	ANDA075932	Epic Pharma LLC	BUPROPION HYDROCHLORIDE	150 mg/1	250 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-415-52)
42806-415-60	42806-415	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20211215	N/A	ANDA	ANDA075932	Epic Pharma LLC	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-415-60)
50090-6353-0	50090-6353	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20230201	N/A	ANDA	ANDA075932	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6353-0)
50090-6353-1	50090-6353	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20230201	N/A	ANDA	ANDA075932	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6353-1)
50090-6353-2	50090-6353	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20230201	N/A	ANDA	ANDA075932	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6353-2)
50090-6353-3	50090-6353	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20230201	N/A	ANDA	ANDA075932	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6353-3)
50090-6354-0	50090-6354	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20230201	N/A	ANDA	ANDA075932	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	150 mg/1	29 BLISTER PACK in 1 CARTON (50090-6354-0) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
71335-0019-1	71335-0019	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20181207	20250731	ANDA	ANDA075932	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0019-1)
71335-0019-2	71335-0019	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180918	20250731	ANDA	ANDA075932	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0019-2)
71335-0019-3	71335-0019	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190321	20250731	ANDA	ANDA075932	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0019-3)
71335-0019-4	71335-0019	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220628	20250731	ANDA	ANDA075932	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0019-4)
71335-0019-5	71335-0019	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220628	20250731	ANDA	ANDA075932	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0019-5)
71335-0019-6	71335-0019	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220628	20250731	ANDA	ANDA075932	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	100 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0019-6)
50090-6743-0	50090-6743	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20231016	N/A	ANDA	ANDA075932	A-S Medication Solutions	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6743-0)