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=ANDA206200"
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
65162-778-10 65162-778 HUMAN PRESCRIPTION DRUG Budesonide Budesonide CAPSULE, DELAYED RELEASE ORAL 20170915 N/A ANDA ANDA206200 Amneal Pharmaceuticals LLC BUDESONIDE 3 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65162-778-10)
65162-778-18 65162-778 HUMAN PRESCRIPTION DRUG Budesonide Budesonide CAPSULE, DELAYED RELEASE ORAL 20170915 N/A ANDA ANDA206200 Amneal Pharmaceuticals LLC BUDESONIDE 3 mg/1 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65162-778-18)
65162-778-30 65162-778 HUMAN PRESCRIPTION DRUG Budesonide Budesonide CAPSULE, DELAYED RELEASE ORAL 20170915 N/A ANDA ANDA206200 Amneal Pharmaceuticals LLC BUDESONIDE 3 mg/1 300 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65162-778-30)
65162-778-49 65162-778 HUMAN PRESCRIPTION DRUG Budesonide Budesonide CAPSULE, DELAYED RELEASE ORAL 20170915 N/A ANDA ANDA206200 Amneal Pharmaceuticals LLC BUDESONIDE 3 mg/1 21 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65162-778-49)
0904-7166-10 0904-7166 HUMAN PRESCRIPTION DRUG Budesonide Budesonide CAPSULE, DELAYED RELEASE ORAL 20170915 N/A ANDA ANDA206200 Major Pharmaceuticals BUDESONIDE 3 mg/1 20 BLISTER PACK in 1 CARTON (0904-7166-10) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
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