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
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)
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)
71205-387-30	71205-387	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200115	N/A	ANDA	ANDA075932	Proficient Rx LP	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-387-30)
71205-387-60	71205-387	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200115	N/A	ANDA	ANDA075932	Proficient Rx LP	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-387-60)
71205-387-90	71205-387	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200115	N/A	ANDA	ANDA075932	Proficient Rx LP	BUPROPION HYDROCHLORIDE	100 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-387-90)
70518-3905-0	70518-3905	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20231103	N/A	ANDA	ANDA075932	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3905-0)
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
0185-0410-01	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)
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)
0185-0415-05	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)
0185-0415-52	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)
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)