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=ANDA202050"
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
65862-561-99 65862-561 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 2.5 mg/1 1000 TABLET in 1 BOTTLE (65862-561-99)
65862-562-01 65862-562 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 5 mg/1 100 TABLET in 1 BOTTLE (65862-562-01)
65862-562-10 65862-562 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 5 mg/1 10 BLISTER PACK in 1 CARTON (65862-562-10) / 10 TABLET in 1 BLISTER PACK
65862-562-30 65862-562 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 5 mg/1 30 TABLET in 1 BOTTLE (65862-562-30)
65862-562-99 65862-562 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 5 mg/1 1000 TABLET in 1 BOTTLE (65862-562-99)
65862-563-01 65862-563 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 7.5 mg/1 100 TABLET in 1 BOTTLE (65862-563-01)
65862-563-05 65862-563 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 7.5 mg/1 500 TABLET in 1 BOTTLE (65862-563-05)
65862-563-10 65862-563 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 7.5 mg/1 10 BLISTER PACK in 1 CARTON (65862-563-10) / 10 TABLET in 1 BLISTER PACK
65862-563-30 65862-563 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 7.5 mg/1 30 TABLET in 1 BOTTLE (65862-563-30)
65862-563-99 65862-563 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 7.5 mg/1 1000 TABLET in 1 BOTTLE (65862-563-99)
65862-564-01 65862-564 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 10 mg/1 100 TABLET in 1 BOTTLE (65862-564-01)
65862-564-10 65862-564 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 10 mg/1 10 BLISTER PACK in 1 CARTON (65862-564-10) / 10 TABLET in 1 BLISTER PACK
65862-564-30 65862-564 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 10 mg/1 30 TABLET in 1 BOTTLE (65862-564-30)
65862-564-99 65862-564 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 10 mg/1 1000 TABLET in 1 BOTTLE (65862-564-99)
65862-565-01 65862-565 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 15 mg/1 100 TABLET in 1 BOTTLE (65862-565-01)
65862-565-10 65862-565 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 15 mg/1 10 BLISTER PACK in 1 CARTON (65862-565-10) / 10 TABLET in 1 BLISTER PACK
65862-565-30 65862-565 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 15 mg/1 30 TABLET in 1 BOTTLE (65862-565-30)
65862-565-99 65862-565 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 15 mg/1 1000 TABLET in 1 BOTTLE (65862-565-99)
65862-566-01 65862-566 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 20 mg/1 100 TABLET in 1 BOTTLE (65862-566-01)
65862-566-05 65862-566 HUMAN PRESCRIPTION DRUG Olanzapine Olanzapine TABLET ORAL 20120423 N/A ANDA ANDA202050 Aurobindo Pharma Limited OLANZAPINE 20 mg/1 500 TABLET in 1 BOTTLE (65862-566-05)
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