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
61919-136-30	61919-136	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20220421	N/A	ANDA	ANDA075932	Direct_Rx	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-136-30)
61919-136-60	61919-136	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20220421	N/A	ANDA	ANDA075932	Direct_Rx	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-136-60)
0185-1111-60	0185-1111	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20050622	20250331	ANDA	ANDA075932	Eon Labs, Inc.	BUPROPION HYDROCHLORIDE	200 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0185-1111-60)
0904-6585-61	0904-6585	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20040322	N/A	ANDA	ANDA075932	Major Pharmaceuticals	BUPROPION HYDROCHLORIDE	150 mg/1	100 BLISTER PACK in 1 CARTON (0904-6585-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0185-0415-05	0185-0415	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20040322	20250430	ANDA	ANDA075932	Eon Labs, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (0185-0415-05)
0185-0415-01	0185-0415	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20040322	20250731	ANDA	ANDA075932	Eon Labs, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0185-0415-01)
0185-0415-52	0185-0415	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20040322	20240930	ANDA	ANDA075932	Eon Labs, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	250 TABLET, EXTENDED RELEASE in 1 BOTTLE (0185-0415-52)
0185-0415-60	0185-0415	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20040322	20240930	ANDA	ANDA075932	Eon Labs, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0185-0415-60)
42806-415-01	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	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-415-01)
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
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)
0185-0410-01	0185-0410	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20031125	20250531	ANDA	ANDA075932	Eon Labs, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0185-0410-01)
0185-0410-05	0185-0410	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20031125	20240930	ANDA	ANDA075932	Eon Labs, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (0185-0410-05)
0185-0410-60	0185-0410	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20031125	20250531	ANDA	ANDA075932	Eon Labs, Inc.	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0185-0410-60)
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)