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 3 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
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)
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)
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)
60505-0157-1 60505-0157 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Apotex Corp BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (60505-0157-1)
60505-0157-3 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 30 TABLET, FILM COATED in 1 BOTTLE (60505-0157-3)
60505-0157-5 60505-0157 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Apotex Corp BUPROPION HYDROCHLORIDE 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (60505-0157-5)
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)
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)
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)
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