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=ANDA075909"
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
55111-134-10 55111-134 HUMAN PRESCRIPTION DRUG Enalapril maleate and hydrochlorothiazide Enalapril maleate and hydrochlorothiazide TABLET ORAL 20011015 N/A ANDA ANDA075909 Dr. Reddy's Laboratories Limited ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE 10 mg/1; 25 mg/1 1000 TABLET in 1 BOTTLE (55111-134-10)
55111-134-01 55111-134 HUMAN PRESCRIPTION DRUG Enalapril maleate and hydrochlorothiazide Enalapril maleate and hydrochlorothiazide TABLET ORAL 20011015 N/A ANDA ANDA075909 Dr. Reddy's Laboratories Limited ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE 10 mg/1; 25 mg/1 100 TABLET in 1 BOTTLE (55111-134-01)
55111-133-10 55111-133 HUMAN PRESCRIPTION DRUG Enalapril maleate and hydrochlorothiazide Enalapril maleate and hydrochlorothiazide TABLET ORAL 20011015 N/A ANDA ANDA075909 Dr. Reddy's Laboratories Limited ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE 5 mg/1; 12.5 mg/1 1000 TABLET in 1 BOTTLE (55111-133-10)
55111-133-01 55111-133 HUMAN PRESCRIPTION DRUG Enalapril maleate and hydrochlorothiazide Enalapril maleate and hydrochlorothiazide TABLET ORAL 20011015 N/A ANDA ANDA075909 Dr. Reddy's Laboratories Limited ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE 5 mg/1; 12.5 mg/1 100 TABLET in 1 BOTTLE (55111-133-01)
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