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=ANDA075682"
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
68788-9112-7 68788-9112 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Preferred Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 21 TABLET in 1 BOTTLE (68788-9112-7)
68788-9112-8 68788-9112 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Preferred Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 120 TABLET in 1 BOTTLE (68788-9112-8)
68788-9112-9 68788-9112 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Preferred Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 90 TABLET in 1 BOTTLE (68788-9112-9)
68788-9110-5 68788-9110 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Preferred Pharmaceuticals, Inc. IBUPROFEN 400 mg/1 50 TABLET in 1 BOTTLE (68788-9110-5)
68788-9110-1 68788-9110 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Preferred Pharmaceuticals, Inc. IBUPROFEN 400 mg/1 100 TABLET in 1 BOTTLE (68788-9110-1)
68788-9110-2 68788-9110 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Preferred Pharmaceuticals, Inc. IBUPROFEN 400 mg/1 20 TABLET in 1 BOTTLE (68788-9110-2)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase