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=ANDA070033"
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
63187-035-28 63187-035 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20240823 N/A ANDA ANDA070033 Proficient Rx LP METRONIDAZOLE 500 mg/1 28 TABLET in 1 BOTTLE (63187-035-28)
63187-035-30 63187-035 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20181101 N/A ANDA ANDA070033 Proficient Rx LP METRONIDAZOLE 500 mg/1 30 TABLET in 1 BOTTLE (63187-035-30)
70518-1241-0 70518-1241 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20180601 N/A ANDA ANDA070033 REMEDYREPACK INC. METRONIDAZOLE 500 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (70518-1241-0)
70518-1241-2 70518-1241 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20210924 N/A ANDA ANDA070033 REMEDYREPACK INC. METRONIDAZOLE 500 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (70518-1241-2)
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