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=ANDA215796"
符合检索条件的记录共 3 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
50742-611-01 50742-611 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, EXTENDED RELEASE ORAL 20250601 N/A ANDA ANDA215796 Ingenus Pharmaceuticals, LLC OXCARBAZEPINE 150 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50742-611-01)
50742-612-01 50742-612 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, EXTENDED RELEASE ORAL 20250601 N/A ANDA ANDA215796 Ingenus Pharmaceuticals, LLC OXCARBAZEPINE 300 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50742-612-01)
50742-613-01 50742-613 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, EXTENDED RELEASE ORAL 20250601 N/A ANDA ANDA215796 Ingenus Pharmaceuticals, LLC OXCARBAZEPINE 600 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50742-613-01)
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