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
60687-340-01 60687-340 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20180201 N/A ANDA ANDA076143 American Health Packaging BUPROPION HYDROCHLORIDE 75 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-340-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-340-11)
70518-1584-0 70518-1584 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20181024 N/A ANDA ANDA076143 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1584-0)
70518-1584-1 70518-1584 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20190219 N/A ANDA ANDA076143 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1584-1)
43063-880-30 43063-880 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20180813 N/A ANDA ANDA076143 PD-Rx Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-880-30)
43063-880-60 43063-880 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20181030 N/A ANDA ANDA076143 PD-Rx Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 75 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-880-60)
45865-473-30 45865-473 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20210908 N/A ANDA ANDA076143 Medsource Pharmaceuticals BUPROPION HYDROCHLORIDE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (45865-473-30)
50268-143-15 50268-143 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20170802 N/A ANDA ANDA076143 AvPAK BUPROPION HYDROCHLORIDE 100 mg/1 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-143-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-143-11)
72789-070-30 72789-070 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20200326 N/A ANDA ANDA076143 PD-Rx Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-30)
72789-070-90 72789-070 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240607 N/A ANDA ANDA076143 PD-Rx Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-90)
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
68001-309-00 68001-309 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20170208 N/A ANDA ANDA076143 BluePoint Laboratories BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68001-309-00)
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)
82804-127-30 82804-127 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240718 N/A ANDA ANDA076143 Proficient Rx LP BUPROPION HYDROCHLORIDE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (82804-127-30)
71610-774-53 71610-774 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240122 N/A ANDA ANDA076143 Aphena Pharma Solutions - Tennessee, LLC BUPROPION HYDROCHLORIDE 75 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71610-774-53)
60687-351-01 60687-351 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20180201 N/A ANDA ANDA076143 American Health Packaging BUPROPION HYDROCHLORIDE 100 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-351-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-351-11)
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)
68071-2577-3 68071-2577 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20211117 N/A ANDA ANDA076143 NuCare Pharmaceuticals,Inc. BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-2577-3)
68001-308-00 68001-308 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20170208 N/A ANDA ANDA076143 BluePoint Laboratories BUPROPION HYDROCHLORIDE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68001-308-00)
60429-746-01 60429-746 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20190822 N/A ANDA ANDA076143 Golden State Medical Supply, Inc. BUPROPION HYDROCHLORIDE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (60429-746-01)
82804-123-30 82804-123 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240715 N/A ANDA ANDA076143 Proficient Rx LP BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (82804-123-30)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase