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 254 条，共 13 页，当前第 2 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
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)
42708-175-30 42708-175 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230620 N/A ANDA ANDA091625 QPharma Inc IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-175-30)
70010-068-01 70010-068 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260218 N/A ANDA ANDA091625 Granules Pharmaceuticals Inc. IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70010-068-01)
70010-068-03 70010-068 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260218 N/A ANDA ANDA091625 Granules Pharmaceuticals Inc. IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70010-068-03)
70010-068-05 70010-068 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260218 N/A ANDA ANDA091625 Granules Pharmaceuticals Inc. IBUPROFEN 800 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (70010-068-05)
70010-068-10 70010-068 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260218 N/A ANDA ANDA091625 Granules Pharmaceuticals Inc. IBUPROFEN 800 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70010-068-10)
67877-320-01 67877-320 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151221 N/A ANDA ANDA091625 Ascend Laboratories, LLC IBUPROFEN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (67877-320-01)
67877-320-05 67877-320 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151221 N/A ANDA ANDA091625 Ascend Laboratories, LLC IBUPROFEN 600 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (67877-320-05)
67877-320-30 67877-320 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151221 N/A ANDA ANDA091625 Ascend Laboratories, LLC IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (67877-320-30)
67877-320-50 67877-320 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151221 N/A ANDA ANDA091625 Ascend Laboratories, LLC IBUPROFEN 600 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (67877-320-50)
72789-382-30 72789-382 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240221 N/A ANDA ANDA091625 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-382-30)
70010-067-01 70010-067 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260218 N/A ANDA ANDA091625 Granules Pharmaceuticals Inc. IBUPROFEN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70010-067-01)
70010-067-03 70010-067 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260218 N/A ANDA ANDA091625 Granules Pharmaceuticals Inc. IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70010-067-03)
70010-067-05 70010-067 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260218 N/A ANDA ANDA091625 Granules Pharmaceuticals Inc. IBUPROFEN 600 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (70010-067-05)
70010-067-10 70010-067 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260218 N/A ANDA ANDA091625 Granules Pharmaceuticals Inc. IBUPROFEN 600 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70010-067-10)
63187-980-90 63187-980 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20180201 N/A ANDA ANDA091625 Proficient Rx LP IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-980-90)
51655-385-20 51655-385 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 800 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-20)
51655-385-21 51655-385 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20200521 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 800 mg/1 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-21)
51655-385-25 51655-385 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230407 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-25)
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