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)
检索条件:" 注册申请号=ANDA076143"
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
60505-0157-9 60505-0157 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Apotex Corp BUPROPION HYDROCHLORIDE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (60505-0157-9)
0904-6635-61 0904-6635 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Major Pharmaceuticals BUPROPION HYDROCHLORIDE 75 mg/1 100 BLISTER PACK in 1 CARTON (0904-6635-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
55154-4152-0 55154-4152 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20220518 N/A ANDA ANDA076143 Cardinal Health 107, LLC BUPROPION HYDROCHLORIDE 75 mg/1 10 BLISTER PACK in 1 BAG (55154-4152-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
70518-1566-0 70518-1566 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20181222 N/A ANDA ANDA076143 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 75 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1566-0)
60760-781-30 60760-781 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20250521 N/A ANDA ANDA076143 ST. MARY'S MEDICAL PARK PHARMACY BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-781-30)
71610-774-80 71610-774 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240125 N/A ANDA ANDA076143 Aphena Pharma Solutions - Tennessee, LLC BUPROPION HYDROCHLORIDE 75 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71610-774-80)
71610-774-94 71610-774 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240125 N/A ANDA ANDA076143 Aphena Pharma Solutions - Tennessee, LLC BUPROPION HYDROCHLORIDE 75 mg/1 360 TABLET, FILM COATED in 1 BOTTLE (71610-774-94)
50090-1869-0 50090-1869 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20150610 N/A ANDA ANDA076143 A-S Medication Solutions BUPROPION HYDROCHLORIDE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-1869-0)
50090-1869-3 50090-1869 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20150610 N/A ANDA ANDA076143 A-S Medication Solutions BUPROPION HYDROCHLORIDE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-1869-3)
60429-747-01 60429-747 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20190822 N/A ANDA ANDA076143 Golden State Medical Supply, Inc. BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (60429-747-01)
68071-2256-1 68071-2256 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20200910 N/A ANDA ANDA076143 NuCare Pharmaceuticals,Inc. BUPROPION HYDROCHLORIDE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68071-2256-1)
0904-6636-61 0904-6636 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Major Pharmaceuticals BUPROPION HYDROCHLORIDE 100 mg/1 100 BLISTER PACK in 1 CARTON (0904-6636-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
71335-0013-1 71335-0013 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20180308 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0013-1)
71335-0013-2 71335-0013 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20180221 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 75 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0013-2)
72189-457-30 72189-457 HUMAN PRESCRIPTION DRUG Bupropion HCL Bupropion HCL TABLET, FILM COATED ORAL 20230330 N/A ANDA ANDA076143 Direct_Rx BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-457-30)
71335-0013-3 71335-0013 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240709 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 75 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0013-3)
71335-0013-4 71335-0013 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240709 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 75 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (71335-0013-4)
71335-0013-5 71335-0013 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240709 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 75 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (71335-0013-5)
71335-0013-6 71335-0013 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240709 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 75 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-0013-6)
71335-0013-7 71335-0013 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240709 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-0013-7)
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