美国药品NDC数据库(National Drug Code Database)=>当前查询条件:"申请号:NDA020648;",共 9 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
66490-650HUMAN PRESCRIPTION DRUGDiastatdiazepamGELRECTAL19970729NDANDA020648Bausch Health US, LLCDIAZEPAM2.5mg/.5mL
0187-0658HUMAN PRESCRIPTION DRUGDiastatdiazepamGELRECTAL19970729NDANDA020648Bausch Health US LLCDIAZEPAM10mg/2mL
0187-0659HUMAN PRESCRIPTION DRUGDiastatdiazepamGELRECTAL19970729NDANDA020648Bausch Health US LLCDIAZEPAM20mg/4mL
68682-650HUMAN PRESCRIPTION DRUGDiazepamDiazepamGELRECTAL19970729NDA AUTHORIZED GENERICNDA020648Oceanside PharmaceuticalsDIAZEPAM2.5mg/.5mL
68682-652HUMAN PRESCRIPTION DRUGDiazepamdiazepamGELRECTAL19970729NDA AUTHORIZED GENERICNDA020648Oceanside PharmaceuticalsDIAZEPAM10mg/2mL
68682-655HUMAN PRESCRIPTION DRUGDiazepamDiazepamGELRECTAL19970729NDA AUTHORIZED GENERICNDA020648Oceanside PharmaceuticalsDIAZEPAM20mg/4mL
0093-6137HUMAN PRESCRIPTION DRUGDiazepamDiazepamGELRECTAL20101001(已中止上市,日期20201031)NDA AUTHORIZED GENERICNDA020648Teva Pharmaceuticals USA, Inc.DIAZEPAM2.5mg/.5mL
0093-6138HUMAN PRESCRIPTION DRUGDiazepamDiazepamGELRECTAL20100903(已中止上市,日期20211031)NDA AUTHORIZED GENERICNDA020648Teva Pharmaceuticals USA, Inc.DIAZEPAM10mg/2mL
0093-6139HUMAN PRESCRIPTION DRUGDiazepamDiazepamGELRECTAL20100903(已中止上市,日期20210930)NDA AUTHORIZED GENERICNDA020648Teva Pharmaceuticals USA, Inc.DIAZEPAM20mg/4mL