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=ANDA202284"
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
63629-1937-1 63629-1937 HUMAN PRESCRIPTION DRUG Felbamate Felbamate TABLET ORAL 20210114 N/A ANDA ANDA202284 Bryant Ranch Prepack FELBAMATE 400 mg/1 100 TABLET in 1 BOTTLE (63629-1937-1)
63629-1944-1 63629-1944 HUMAN PRESCRIPTION DRUG Felbamate Felbamate TABLET ORAL 20210119 N/A ANDA ANDA202284 Bryant Ranch Prepack FELBAMATE 600 mg/1 100 TABLET in 1 BOTTLE (63629-1944-1)
62559-731-01 62559-731 HUMAN PRESCRIPTION DRUG Felbamate Felbamate TABLET ORAL 20180904 N/A ANDA ANDA202284 ANI Pharmaceuticals, Inc. FELBAMATE 600 mg/1 100 TABLET in 1 BOTTLE (62559-731-01)
62559-730-01 62559-730 HUMAN PRESCRIPTION DRUG Felbamate Felbamate TABLET ORAL 20180904 N/A ANDA ANDA202284 ANI Pharmaceuticals, Inc. FELBAMATE 400 mg/1 100 TABLET in 1 BOTTLE (62559-730-01)
72162-1771-1 72162-1771 HUMAN PRESCRIPTION DRUG Felbamate Felbamate TABLET ORAL 20230830 N/A ANDA ANDA202284 Bryant Ranch Prepack FELBAMATE 600 mg/1 100 TABLET in 1 BOTTLE (72162-1771-1)
72162-1770-1 72162-1770 HUMAN PRESCRIPTION DRUG Felbamate Felbamate TABLET ORAL 20230830 N/A ANDA ANDA202284 Bryant Ranch Prepack FELBAMATE 400 mg/1 100 TABLET in 1 BOTTLE (72162-1770-1)
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