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=ANDA213794"
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
80425-0424-2 80425-0424 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240801 N/A ANDA ANDA213794 Advanced Rx of Tennessee, LLC IBUPROFEN 600 mg/1 60 TABLET in 1 BOTTLE (80425-0424-2)
80425-0424-3 80425-0424 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240801 N/A ANDA ANDA213794 Advanced Rx of Tennessee, LLC IBUPROFEN 600 mg/1 90 TABLET in 1 BOTTLE (80425-0424-3)
80425-0424-4 80425-0424 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240801 N/A ANDA ANDA213794 Advanced Rx of Tennessee, LLC IBUPROFEN 600 mg/1 100 TABLET in 1 BOTTLE (80425-0424-4)
50090-5435-9 50090-5435 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20210118 N/A ANDA ANDA213794 A-S Medication Solutions IBUPROFEN 600 mg/1 24 TABLET in 1 BOTTLE (50090-5435-9)
68071-2947-1 68071-2947 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230303 N/A ANDA ANDA213794 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 21 TABLET in 1 BOTTLE (68071-2947-1)
68071-2947-2 68071-2947 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230303 N/A ANDA ANDA213794 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 20 TABLET in 1 BOTTLE (68071-2947-2)
68071-2947-3 68071-2947 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230303 N/A ANDA ANDA213794 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 30 TABLET in 1 BOTTLE (68071-2947-3)
68071-2947-4 68071-2947 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20251030 N/A ANDA ANDA213794 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 40 TABLET in 1 BOTTLE (68071-2947-4)
68071-2947-5 68071-2947 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230303 N/A ANDA ANDA213794 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 50 TABLET in 1 BOTTLE (68071-2947-5)
68071-2947-6 68071-2947 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230303 N/A ANDA ANDA213794 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 60 TABLET in 1 BOTTLE (68071-2947-6)
68071-2947-9 68071-2947 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230303 N/A ANDA ANDA213794 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 90 TABLET in 1 BOTTLE (68071-2947-9)
68071-3696-8 68071-3696 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20241008 N/A ANDA ANDA213794 NuCare Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 180 TABLET in 1 BOTTLE (68071-3696-8)
68788-8319-1 68788-8319 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20221223 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 100 TABLET in 1 BOTTLE (68788-8319-1)
68788-8319-2 68788-8319 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20221223 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 20 TABLET in 1 BOTTLE (68788-8319-2)
68788-8319-3 68788-8319 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20221223 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 30 TABLET in 1 BOTTLE (68788-8319-3)
68788-8319-4 68788-8319 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20221223 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 14 TABLET in 1 BOTTLE (68788-8319-4)
68788-8319-5 68788-8319 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20221223 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 50 TABLET in 1 BOTTLE (68788-8319-5)
68788-8319-6 68788-8319 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20221223 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 60 TABLET in 1 BOTTLE (68788-8319-6)
68788-8319-7 68788-8319 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20221223 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 21 TABLET in 1 BOTTLE (68788-8319-7)
68788-8319-8 68788-8319 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20221223 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 120 TABLET in 1 BOTTLE (68788-8319-8)
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