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=ANDA209675"
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
50742-247-05 50742-247 HUMAN PRESCRIPTION DRUG Clonidine clonidine TABLET, EXTENDED RELEASE ORAL 20190305 N/A ANDA ANDA209675 Ingenus Pharmaceuticals, LLC CLONIDINE HYDROCHLORIDE .1 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-247-05)
50742-247-30 50742-247 HUMAN PRESCRIPTION DRUG Clonidine clonidine TABLET, EXTENDED RELEASE ORAL 20190305 N/A ANDA ANDA209675 Ingenus Pharmaceuticals, LLC CLONIDINE HYDROCHLORIDE .1 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-247-30)
50742-247-60 50742-247 HUMAN PRESCRIPTION DRUG Clonidine clonidine TABLET, EXTENDED RELEASE ORAL 20190305 N/A ANDA ANDA209675 Ingenus Pharmaceuticals, LLC CLONIDINE HYDROCHLORIDE .1 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-247-60)
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