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=ANDA208681"
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
15955-389-01 15955-389 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20190626 N/A ANDA ANDA208681 Alembic Labs LLC METRONIDAZOLE 500 mg/1 100 TABLET in 1 BOTTLE (15955-389-01)
15955-389-05 15955-389 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20190626 N/A ANDA ANDA208681 Alembic Labs LLC METRONIDAZOLE 500 mg/1 500 TABLET in 1 BOTTLE (15955-389-05)
15955-388-01 15955-388 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20190626 N/A ANDA ANDA208681 Alembic Labs LLC METRONIDAZOLE 250 mg/1 100 TABLET in 1 BOTTLE (15955-388-01)
15955-388-05 15955-388 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20190626 N/A ANDA ANDA208681 Alembic Labs LLC METRONIDAZOLE 250 mg/1 500 TABLET in 1 BOTTLE (15955-388-05)
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