美国药品NDC数据库(National Drug Code Database)=>当前查询条件:"申请号:ANDA040621;",共 7 条结果。点击左侧“产品NDC”可以查询指定剂量规格药品的所有包装规格及药品说明书。
产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 市场分类 申请号 标签持有者 活性成分 规格 规格单位
71335-0232HUMAN PRESCRIPTION DRUGPHENYTOIN SODIUMPHENYTOIN SODIUMCAPSULE, EXTENDED RELEASEORAL20061212ANDAANDA040621Bryant Ranch PrepackPHENYTOIN SODIUM100mg/1
63187-891HUMAN PRESCRIPTION DRUGPHENYTOIN SODIUMPHENYTOIN SODIUMCAPSULE, EXTENDED RELEASEORAL20061212ANDAANDA040621Proficient Rx LPPHENYTOIN SODIUM100mg/1
70518-0981HUMAN PRESCRIPTION DRUGPHENYTOIN SODIUMPHENYTOIN SODIUMCAPSULE, EXTENDED RELEASEORAL20180122ANDAANDA040621REMEDYREPACK INC.PHENYTOIN SODIUM100mg/1
62756-402HUMAN PRESCRIPTION DRUGPHENYTOIN SODIUMPHENYTOIN SODIUMCAPSULE, EXTENDED RELEASEORAL20061212ANDAANDA040621Sun Pharmaceutical Industries, Inc.PHENYTOIN SODIUM100mg/1
53002-1501HUMAN PRESCRIPTION DRUGPHENYTOIN SODIUMPHENYTOIN SODIUMCAPSULE, EXTENDED RELEASEORAL20061212ANDAANDA040621RPK Pharmaceuticals, Inc.PHENYTOIN SODIUM100mg/1
63629-6364HUMAN PRESCRIPTION DRUGPHENYTOIN SODIUMPHENYTOIN SODIUMCAPSULE, EXTENDED RELEASEORAL20061212ANDAANDA040621Bryant Ranch PrepackPHENYTOIN SODIUM100mg/1
63629-6382HUMAN PRESCRIPTION DRUGPHENYTOIN SODIUMPHENYTOIN SODIUMCAPSULE, EXTENDED RELEASEORAL20061212ANDAANDA040621Bryant Ranch PrepackPHENYTOIN SODIUM100mg/1