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=ANDA205689"
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
63629-8161-1 63629-8161 HUMAN PRESCRIPTION DRUG Guanfacine Guanfacine TABLET, EXTENDED RELEASE ORAL 20190702 N/A ANDA ANDA205689 Bryant Ranch Prepack GUANFACINE HYDROCHLORIDE 1 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8161-1)
63304-925-01 63304-925 HUMAN PRESCRIPTION DRUG Guanfacine Guanfacine TABLET, EXTENDED RELEASE ORAL 20180817 N/A ANDA ANDA205689 Sun Pharmaceutical Industries, Inc GUANFACINE HYDROCHLORIDE 2 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-925-01)
63304-925-05 63304-925 HUMAN PRESCRIPTION DRUG Guanfacine Guanfacine TABLET, EXTENDED RELEASE ORAL 20180817 N/A ANDA ANDA205689 Sun Pharmaceutical Industries, Inc GUANFACINE HYDROCHLORIDE 2 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-925-05)
63304-925-30 63304-925 HUMAN PRESCRIPTION DRUG Guanfacine Guanfacine TABLET, EXTENDED RELEASE ORAL 20180817 N/A ANDA ANDA205689 Sun Pharmaceutical Industries, Inc GUANFACINE HYDROCHLORIDE 2 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-925-30)
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