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=ANDA071268"
符合检索条件的记录共 44 条，共 3 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
68788-8244-6 68788-8244 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220809 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8244-6)
68788-8244-7 68788-8244 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220809 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (68788-8244-7)
68788-8244-8 68788-8244 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220809 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (68788-8244-8)
68788-8244-9 68788-8244 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220809 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8244-9)
68788-8278-4 68788-8278 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230713 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (68788-8278-4)
68071-2756-2 68071-2756 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220615 N/A ANDA ANDA071268 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68071-2756-2)
68071-2756-5 68071-2756 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220615 N/A ANDA ANDA071268 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (68071-2756-5)
68788-8278-1 68788-8278 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230713 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-8278-1)
68788-8278-2 68788-8278 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230713 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68788-8278-2)
68788-8278-3 68788-8278 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230713 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8278-3)
68788-8278-5 68788-8278 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230713 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (68788-8278-5)
68788-8278-6 68788-8278 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230713 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8278-6)
68788-8278-7 68788-8278 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230713 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (68788-8278-7)
68788-8278-8 68788-8278 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230713 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (68788-8278-8)
68788-8278-9 68788-8278 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230713 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8278-9)
68788-8201-1 68788-8201 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220523 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-8201-1)
68788-8201-2 68788-8201 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220523 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68788-8201-2)
68788-8201-3 68788-8201 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220523 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8201-3)
68788-8201-5 68788-8201 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220523 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (68788-8201-5)
68788-8201-6 68788-8201 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220523 N/A ANDA ANDA071268 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8201-6)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase