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=ANDA211919"
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
16571-735-01 16571-735 HUMAN PRESCRIPTION DRUG Methylergonovine Maleate Methylergonovine Maleate TABLET ORAL 20210115 N/A ANDA ANDA211919 Rising Pharma Holdings, Inc. METHYLERGONOVINE MALEATE .2 mg/1 100 TABLET in 1 BOTTLE (16571-735-01)
16571-735-17 16571-735 HUMAN PRESCRIPTION DRUG Methylergonovine Maleate Methylergonovine Maleate TABLET ORAL 20210115 N/A ANDA ANDA211919 Rising Pharma Holdings, Inc. METHYLERGONOVINE MALEATE .2 mg/1 7 TABLET in 1 BOTTLE (16571-735-17)
16571-735-21 16571-735 HUMAN PRESCRIPTION DRUG Methylergonovine Maleate Methylergonovine Maleate TABLET ORAL 20210115 N/A ANDA ANDA211919 Rising Pharma Holdings, Inc. METHYLERGONOVINE MALEATE .2 mg/1 12 TABLET in 1 BOTTLE (16571-735-21)
16571-735-28 16571-735 HUMAN PRESCRIPTION DRUG Methylergonovine Maleate Methylergonovine Maleate TABLET ORAL 20210115 N/A ANDA ANDA211919 Rising Pharma Holdings, Inc. METHYLERGONOVINE MALEATE .2 mg/1 28 TABLET in 1 BOTTLE (16571-735-28)
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