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=ANDA075682"
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
0904-5854-40 0904-5854 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20090610 N/A ANDA ANDA075682 Major Pharmaceuticals IBUPROFEN 600 mg/1 500 TABLET in 1 BOTTLE (0904-5854-40)
0904-5853-40 0904-5853 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20090610 N/A ANDA ANDA075682 Major Pharmaceuticals IBUPROFEN 400 mg/1 500 TABLET in 1 BOTTLE (0904-5853-40)
55111-682-01 55111-682 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 400 mg/1 100 TABLET in 1 BOTTLE (55111-682-01)
55111-682-05 55111-682 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 400 mg/1 500 TABLET in 1 BOTTLE (55111-682-05)
55111-682-09 55111-682 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 400 mg/1 90 TABLET in 1 BOTTLE (55111-682-09)
51407-839-05 51407-839 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250926 N/A ANDA ANDA075682 Golden State Medical Supply, Inc. IBUPROFEN 400 mg/1 500 TABLET in 1 BOTTLE (51407-839-05)
51407-841-01 51407-841 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250926 N/A ANDA ANDA075682 Golden State Medical Supply, Inc. IBUPROFEN 800 mg/1 100 TABLET in 1 BOTTLE (51407-841-01)
51407-841-05 51407-841 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250926 N/A ANDA ANDA075682 Golden State Medical Supply, Inc. IBUPROFEN 800 mg/1 500 TABLET in 1 BOTTLE (51407-841-05)
51407-840-01 51407-840 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250926 N/A ANDA ANDA075682 Golden State Medical Supply, Inc. IBUPROFEN 600 mg/1 100 TABLET in 1 BOTTLE (51407-840-01)
51407-840-05 51407-840 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250926 N/A ANDA ANDA075682 Golden State Medical Supply, Inc. IBUPROFEN 600 mg/1 500 TABLET in 1 BOTTLE (51407-840-05)
51407-839-01 51407-839 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250926 N/A ANDA ANDA075682 Golden State Medical Supply, Inc. IBUPROFEN 400 mg/1 100 TABLET in 1 BOTTLE (51407-839-01)
51655-851-20 51655-851 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20151104 N/A ANDA ANDA075682 Northwind Pharmaceuticals, LLC IBUPROFEN 800 mg/1 20 TABLET in 1 BOTTLE (51655-851-20)
51655-851-51 51655-851 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240116 N/A ANDA ANDA075682 Northwind Pharmaceuticals, LLC IBUPROFEN 800 mg/1 40 TABLET in 1 BOTTLE, PLASTIC (51655-851-51)
55111-683-30 55111-683 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 600 mg/1 30 TABLET in 1 BOTTLE (55111-683-30)
55111-683-50 55111-683 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 600 mg/1 50 TABLET in 1 BOTTLE (55111-683-50)
55111-684-01 55111-684 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 800 mg/1 100 TABLET in 1 BOTTLE (55111-684-01)
55111-684-05 55111-684 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 800 mg/1 500 TABLET in 1 BOTTLE (55111-684-05)
55111-684-09 55111-684 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 800 mg/1 90 TABLET in 1 BOTTLE (55111-684-09)
55111-684-30 55111-684 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 800 mg/1 30 TABLET in 1 BOTTLE (55111-684-30)
55111-684-50 55111-684 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 800 mg/1 50 TABLET in 1 BOTTLE (55111-684-50)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase