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"
符合检索条件的记录共 62 条，共 4 页，当前第 2 页 ，可点击列名称排序
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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
60505-0157-7 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 1000 TABLET, FILM COATED in 1 BOTTLE (60505-0157-7)
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)
60505-0158-1 60505-0158 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Apotex Corp BUPROPION HYDROCHLORIDE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (60505-0158-1)
60505-0158-3 60505-0158 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Apotex Corp BUPROPION HYDROCHLORIDE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (60505-0158-3)
60505-0158-5 60505-0158 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Apotex Corp BUPROPION HYDROCHLORIDE 75 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (60505-0158-5)
60505-0158-7 60505-0158 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Apotex Corp BUPROPION HYDROCHLORIDE 75 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (60505-0158-7)
60505-0158-9 60505-0158 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Apotex Corp BUPROPION HYDROCHLORIDE 75 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (60505-0158-9)
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)
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)
68788-7988-1 68788-7988 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240311 N/A ANDA ANDA076143 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-7988-1)
68788-7988-3 68788-7988 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20210806 N/A ANDA ANDA076143 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-7988-3)
68788-7988-6 68788-7988 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20210806 N/A ANDA ANDA076143 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-7988-6)
68788-7988-9 68788-7988 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20210806 N/A ANDA ANDA076143 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-7988-9)
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)
68071-2577-9 68071-2577 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20250123 N/A ANDA ANDA076143 NuCare Pharmaceuticals,Inc. BUPROPION HYDROCHLORIDE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-2577-9)
72162-2097-1 72162-2097 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72162-2097-1)
72162-2098-1 72162-2098 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72162-2098-1)
50268-142-15 50268-142 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20170802 N/A ANDA ANDA076143 AvPAK BUPROPION HYDROCHLORIDE 75 mg/1 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-142-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-142-11)
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)
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