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=ANDA209119"
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
62332-060-10 62332-060 HUMAN PRESCRIPTION DRUG CANDESARTAN CILEXETIL CANDESARTAN CILEXETIL TABLET ORAL 20170621 N/A ANDA ANDA209119 Alembic Pharmaceuticals Inc. CANDESARTAN CILEXETIL 32 mg/1 100 TABLET in 1 CARTON (62332-060-10)
62332-060-30 62332-060 HUMAN PRESCRIPTION DRUG CANDESARTAN CILEXETIL CANDESARTAN CILEXETIL TABLET ORAL 20170621 N/A ANDA ANDA209119 Alembic Pharmaceuticals Inc. CANDESARTAN CILEXETIL 32 mg/1 30 TABLET in 1 BOTTLE (62332-060-30)
62332-060-90 62332-060 HUMAN PRESCRIPTION DRUG CANDESARTAN CILEXETIL CANDESARTAN CILEXETIL TABLET ORAL 20170621 N/A ANDA ANDA209119 Alembic Pharmaceuticals Inc. CANDESARTAN CILEXETIL 32 mg/1 90 TABLET in 1 BOTTLE (62332-060-90)
46708-060-10 46708-060 HUMAN PRESCRIPTION DRUG CANDESARTAN CILEXETIL CANDESARTAN CILEXETIL TABLET ORAL 20170621 N/A ANDA ANDA209119 Alembic Pharmaceuticals Limited CANDESARTAN CILEXETIL 32 mg/1 100 TABLET in 1 CARTON (46708-060-10)
46708-060-30 46708-060 HUMAN PRESCRIPTION DRUG CANDESARTAN CILEXETIL CANDESARTAN CILEXETIL TABLET ORAL 20170621 N/A ANDA ANDA209119 Alembic Pharmaceuticals Limited CANDESARTAN CILEXETIL 32 mg/1 30 TABLET in 1 BOTTLE (46708-060-30)
46708-060-90 46708-060 HUMAN PRESCRIPTION DRUG CANDESARTAN CILEXETIL CANDESARTAN CILEXETIL TABLET ORAL 20170621 N/A ANDA ANDA209119 Alembic Pharmaceuticals Limited CANDESARTAN CILEXETIL 32 mg/1 90 TABLET in 1 BOTTLE (46708-060-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase