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 228 条，共 12 页，当前第 11 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
70518-0761-2 70518-0761 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20180726 N/A ANDA ANDA091625 REMEDYREPACK INC. IBUPROFEN 600 mg/1 28 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-2)
70518-0761-3 70518-0761 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20180727 N/A ANDA ANDA091625 REMEDYREPACK INC. IBUPROFEN 600 mg/1 21 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-3)
70518-0761-4 70518-0761 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20180730 N/A ANDA ANDA091625 REMEDYREPACK INC. IBUPROFEN 600 mg/1 15 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-4)
67877-319-01 67877-319 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151221 N/A ANDA ANDA091625 Ascend Laboratories, LLC IBUPROFEN 400 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (67877-319-01)
67877-319-05 67877-319 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151221 N/A ANDA ANDA091625 Ascend Laboratories, LLC IBUPROFEN 400 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (67877-319-05)
67877-319-30 67877-319 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151221 N/A ANDA ANDA091625 Ascend Laboratories, LLC IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (67877-319-30)
67877-319-50 67877-319 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151221 N/A ANDA ANDA091625 Ascend Laboratories, LLC IBUPROFEN 400 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (67877-319-50)
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)
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)
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)
70518-1051-0 70518-1051 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20180301 N/A ANDA ANDA091625 REMEDYREPACK INC. IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1051-0)
70518-1051-2 70518-1051 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20201211 N/A ANDA ANDA091625 REMEDYREPACK INC. IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1051-2)
70518-1051-4 70518-1051 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250721 N/A ANDA ANDA091625 REMEDYREPACK INC. IBUPROFEN 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1051-4)
71335-1218-0 71335-1218 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA091625 Bryant Ranch Prepack IBUPROFEN 600 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (71335-1218-0)
71335-1218-1 71335-1218 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA091625 Bryant Ranch Prepack IBUPROFEN 600 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-1218-1)
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