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 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
76282-713-10 76282-713 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76282-713-10)
76282-713-50 76282-713 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 600 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76282-713-50)
76282-713-55 76282-713 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 600 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76282-713-55)
76282-714-10 76282-714 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76282-714-10)
76282-714-30 76282-714 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76282-714-30)
76282-714-46 76282-714 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 800 mg/1 100 BLISTER PACK in 1 CARTON (76282-714-46) / 10 TABLET, FILM COATED in 1 BLISTER PACK (76282-714-45)
76282-714-50 76282-714 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 800 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76282-714-50)
76282-714-55 76282-714 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 800 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76282-714-55)
76282-714-90 76282-714 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76282-714-90)
50090-6645-0 50090-6645 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230829 N/A ANDA ANDA091625 A-S Medication Solutions IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6645-0)
71610-222-60 71610-222 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20190114 N/A ANDA ANDA091625 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71610-222-60)
71610-222-80 71610-222 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20190114 N/A ANDA ANDA091625 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 600 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71610-222-80)
71610-222-92 71610-222 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20190114 N/A ANDA ANDA091625 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 600 mg/1 270 TABLET, FILM COATED in 1 BOTTLE (71610-222-92)
82868-069-30 82868-069 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241120 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-069-30)
82868-069-60 82868-069 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250627 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-069-60)
82868-069-90 82868-069 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241120 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-069-90)
54348-825-00 54348-825 HUMAN PRESCRIPTION DRUG Ibuprofen IBUPROFEN TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA091625 PharmPak, Inc. IBUPROFEN 800 mg/1 1 BOTTLE in 1 BOX (54348-825-00) / 1 TABLET, FILM COATED in 1 BOTTLE
54348-825-06 54348-825 HUMAN PRESCRIPTION DRUG Ibuprofen IBUPROFEN TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA091625 PharmPak, Inc. IBUPROFEN 800 mg/1 1 BOTTLE in 1 BOX (54348-825-06) / 6 TABLET, FILM COATED in 1 BOTTLE
54348-825-08 54348-825 HUMAN PRESCRIPTION DRUG Ibuprofen IBUPROFEN TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA091625 PharmPak, Inc. IBUPROFEN 800 mg/1 1 BOTTLE in 1 BOX (54348-825-08) / 8 TABLET, FILM COATED in 1 BOTTLE
54348-825-09 54348-825 HUMAN PRESCRIPTION DRUG Ibuprofen IBUPROFEN TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA091625 PharmPak, Inc. IBUPROFEN 800 mg/1 1 BOTTLE in 1 BOX (54348-825-09) / 9 TABLET, FILM COATED in 1 BOTTLE
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