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
67296-0913-9 67296-0913 HUMAN PRESCRIPTION DRUG IBU IBU TABLET ORAL 20081120 N/A ANDA ANDA075682 RedPharm Drug, Inc. IBUPROFEN 600 mg/1 90 TABLET in 1 BOTTLE (67296-0913-9)
67296-0913-3 67296-0913 HUMAN PRESCRIPTION DRUG IBU IBU TABLET ORAL 20081120 N/A ANDA ANDA075682 RedPharm Drug, Inc. IBUPROFEN 600 mg/1 10 TABLET in 1 BOTTLE (67296-0913-3)
68071-3053-0 68071-3053 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20180316 N/A ANDA ANDA075682 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 12 TABLET in 1 BOTTLE (68071-3053-0)
68071-3053-1 68071-3053 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20180316 N/A ANDA ANDA075682 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 120 TABLET in 1 BOTTLE (68071-3053-1)
68071-3053-2 68071-3053 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20180316 N/A ANDA ANDA075682 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 20 TABLET in 1 BOTTLE (68071-3053-2)
68071-3053-4 68071-3053 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20180316 N/A ANDA ANDA075682 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 40 TABLET in 1 BOTTLE (68071-3053-4)
68071-3053-6 68071-3053 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20180316 N/A ANDA ANDA075682 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 60 TABLET in 1 BOTTLE (68071-3053-6)
67296-0913-1 67296-0913 HUMAN PRESCRIPTION DRUG IBU IBU TABLET ORAL 20081120 N/A ANDA ANDA075682 RedPharm Drug, Inc. IBUPROFEN 600 mg/1 30 TABLET in 1 BOTTLE (67296-0913-1)
67296-1217-2 67296-1217 HUMAN PRESCRIPTION DRUG IBU IBU TABLET ORAL 20081120 N/A ANDA ANDA075682 RedPharm Drug, Inc. IBUPROFEN 400 mg/1 20 TABLET in 1 BOTTLE (67296-1217-2)
67296-1217-3 67296-1217 HUMAN PRESCRIPTION DRUG IBU IBU TABLET ORAL 20081120 N/A ANDA ANDA075682 RedPharm Drug, Inc. IBUPROFEN 400 mg/1 30 TABLET in 1 BOTTLE (67296-1217-3)
71610-275-92 71610-275 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20190508 N/A ANDA ANDA075682 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 800 mg/1 270 TABLET in 1 BOTTLE (71610-275-92)
71610-275-60 71610-275 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20190508 N/A ANDA ANDA075682 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 800 mg/1 90 TABLET in 1 BOTTLE (71610-275-60)
71610-275-80 71610-275 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20190508 N/A ANDA ANDA075682 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 800 mg/1 180 TABLET in 1 BOTTLE (71610-275-80)
66267-964-00 66267-964 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20170822 N/A ANDA ANDA075682 NuCare Pharmaceuticals Inc. IBUPROFEN 600 mg/1 100 TABLET in 1 BOTTLE (66267-964-00)
66267-963-00 66267-963 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20170915 N/A ANDA ANDA075682 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 100 TABLET in 1 BOTTLE (66267-963-00)
63187-614-28 63187-614 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20191001 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 600 mg/1 28 TABLET in 1 BOTTLE (63187-614-28)
63187-614-40 63187-614 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20170601 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 600 mg/1 40 TABLET in 1 BOTTLE (63187-614-40)
63187-614-42 63187-614 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20200221 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 600 mg/1 42 TABLET in 1 BOTTLE (63187-614-42)
63187-614-45 63187-614 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20160101 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 600 mg/1 45 TABLET in 1 BOTTLE (63187-614-45)
63187-614-60 63187-614 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20160101 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 600 mg/1 60 TABLET in 1 BOTTLE (63187-614-60)
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