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=ANDA091625"
符合检索条件的记录共 245 条，共 13 页，当前第 7 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
50090-2548-3 50090-2548 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20170106 N/A ANDA ANDA091625 A-S Medication Solutions IBUPROFEN 800 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (50090-2548-3)
67877-321-01 67877-321 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151221 N/A ANDA ANDA091625 Ascend Laboratories, LLC IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (67877-321-01)
50090-2549-0 50090-2549 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20181019 N/A ANDA ANDA091625 A-S Medication Solutions IBUPROFEN 800 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (50090-2549-0)
50090-2549-4 50090-2549 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20161107 N/A ANDA ANDA091625 A-S Medication Solutions IBUPROFEN 800 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (50090-2549-4)
50090-2549-5 50090-2549 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20161020 N/A ANDA ANDA091625 A-S Medication Solutions IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-2549-5)
50090-2549-7 50090-2549 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20161020 N/A ANDA ANDA091625 A-S Medication Solutions IBUPROFEN 800 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (50090-2549-7)
67877-321-05 67877-321 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151221 N/A ANDA ANDA091625 Ascend Laboratories, LLC IBUPROFEN 800 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (67877-321-05)
67877-321-30 67877-321 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151221 N/A ANDA ANDA091625 Ascend Laboratories, LLC IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (67877-321-30)
67877-321-50 67877-321 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151221 N/A ANDA ANDA091625 Ascend Laboratories, LLC IBUPROFEN 800 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (67877-321-50)
51655-048-26 51655-048 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20200520 N/A ANDA ANDA091625 Northwind Pharmaceuticals, LLC IBUPROFEN 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-048-26)
51655-048-52 51655-048 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20221014 N/A ANDA ANDA091625 Northwind Pharmaceuticals, LLC IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-048-52)
51655-042-26 51655-042 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20221214 N/A ANDA ANDA091625 Northwind Pharmaceuticals, LLC IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-042-26)
51655-042-52 51655-042 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230628 N/A ANDA ANDA091625 Northwind Pharmaceuticals, LLC IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-042-52)
51655-042-20 51655-042 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230108 N/A ANDA ANDA091625 Northwind Pharmaceuticals, LLC IBUPROFEN 600 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-042-20)
51655-042-25 51655-042 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220909 N/A ANDA ANDA091625 Northwind Pharmaceuticals, LLC IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-042-25)
72789-364-06 72789-364 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240315 N/A ANDA ANDA091625 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-06)
72789-364-21 72789-364 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240111 N/A ANDA ANDA091625 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-21)
72789-364-30 72789-364 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20231114 N/A ANDA ANDA091625 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-30)
72789-364-40 72789-364 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20231115 N/A ANDA ANDA091625 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-40)
72789-364-60 72789-364 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20231113 N/A ANDA ANDA091625 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-60)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase