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=ANDA201049"
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
0781-5634-10 0781-5634 HUMAN PRESCRIPTION DRUG Pioglitazone hydrochloride and glimepiride Pioglitazone hydrochloride and glimepiride TABLET ORAL 20130108 N/A ANDA ANDA201049 Sandoz Inc GLIMEPIRIDE; PIOGLITAZONE HYDROCHLORIDE 2 mg/1; 30 mg/1 1000 TABLET in 1 BOTTLE (0781-5634-10)
0781-5634-31 0781-5634 HUMAN PRESCRIPTION DRUG Pioglitazone hydrochloride and glimepiride Pioglitazone hydrochloride and glimepiride TABLET ORAL 20130108 N/A ANDA ANDA201049 Sandoz Inc GLIMEPIRIDE; PIOGLITAZONE HYDROCHLORIDE 2 mg/1; 30 mg/1 30 TABLET in 1 BOTTLE (0781-5634-31)
0781-5635-10 0781-5635 HUMAN PRESCRIPTION DRUG Pioglitazone hydrochloride and glimepiride Pioglitazone hydrochloride and glimepiride TABLET ORAL 20130108 N/A ANDA ANDA201049 Sandoz Inc GLIMEPIRIDE; PIOGLITAZONE HYDROCHLORIDE 4 mg/1; 30 mg/1 1000 TABLET in 1 BOTTLE (0781-5635-10)
0781-5635-31 0781-5635 HUMAN PRESCRIPTION DRUG Pioglitazone hydrochloride and glimepiride Pioglitazone hydrochloride and glimepiride TABLET ORAL 20130108 N/A ANDA ANDA201049 Sandoz Inc GLIMEPIRIDE; PIOGLITAZONE HYDROCHLORIDE 4 mg/1; 30 mg/1 30 TABLET in 1 BOTTLE (0781-5635-31)
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