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=ANDA074453"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
69367-354-01 69367-354 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET ORAL 20231102 N/A ANDA ANDA074453 Westminster Pharmaceuticals, LLC METOPROLOL TARTRATE 50 mg/1 100 TABLET in 1 BOTTLE (69367-354-01)
69367-354-10 69367-354 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET ORAL 20231102 N/A ANDA ANDA074453 Westminster Pharmaceuticals, LLC METOPROLOL TARTRATE 50 mg/1 1000 TABLET in 1 BOTTLE (69367-354-10)
69367-355-01 69367-355 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET ORAL 20231102 N/A ANDA ANDA074453 Westminster Pharmaceuticals, LLC METOPROLOL TARTRATE 100 mg/1 100 TABLET in 1 BOTTLE (69367-355-01)
69367-355-10 69367-355 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate Metoprolol Tartrate TABLET ORAL 20231102 N/A ANDA ANDA074453 Westminster Pharmaceuticals, LLC METOPROLOL TARTRATE 100 mg/1 1000 TABLET in 1 BOTTLE (69367-355-10)
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