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=ANDA208045"
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
65862-955-05 65862-955 HUMAN PRESCRIPTION DRUG LURASIDONE HYDROCHLORIDE LURASIDONE HYDROCHLORIDE TABLET ORAL 20230310 N/A ANDA ANDA208045 Aurobindo Pharma Limited LURASIDONE HYDROCHLORIDE 60 mg/1 500 TABLET in 1 BOTTLE (65862-955-05)
65862-955-30 65862-955 HUMAN PRESCRIPTION DRUG LURASIDONE HYDROCHLORIDE LURASIDONE HYDROCHLORIDE TABLET ORAL 20230310 N/A ANDA ANDA208045 Aurobindo Pharma Limited LURASIDONE HYDROCHLORIDE 60 mg/1 30 TABLET in 1 BOTTLE (65862-955-30)
65862-955-90 65862-955 HUMAN PRESCRIPTION DRUG LURASIDONE HYDROCHLORIDE LURASIDONE HYDROCHLORIDE TABLET ORAL 20230310 N/A ANDA ANDA208045 Aurobindo Pharma Limited LURASIDONE HYDROCHLORIDE 60 mg/1 90 TABLET in 1 BOTTLE (65862-955-90)
82804-215-30 82804-215 HUMAN PRESCRIPTION DRUG LURASIDONE HYDROCHLORIDE LURASIDONE HYDROCHLORIDE TABLET ORAL 20250331 N/A ANDA ANDA208045 Proficient Rx LP LURASIDONE HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BOTTLE (82804-215-30)
65862-956-05 65862-956 HUMAN PRESCRIPTION DRUG LURASIDONE HYDROCHLORIDE LURASIDONE HYDROCHLORIDE TABLET ORAL 20230310 N/A ANDA ANDA208045 Aurobindo Pharma Limited LURASIDONE HYDROCHLORIDE 80 mg/1 500 TABLET in 1 BOTTLE (65862-956-05)
65862-956-30 65862-956 HUMAN PRESCRIPTION DRUG LURASIDONE HYDROCHLORIDE LURASIDONE HYDROCHLORIDE TABLET ORAL 20230310 N/A ANDA ANDA208045 Aurobindo Pharma Limited LURASIDONE HYDROCHLORIDE 80 mg/1 30 TABLET in 1 BOTTLE (65862-956-30)
65862-956-90 65862-956 HUMAN PRESCRIPTION DRUG LURASIDONE HYDROCHLORIDE LURASIDONE HYDROCHLORIDE TABLET ORAL 20230310 N/A ANDA ANDA208045 Aurobindo Pharma Limited LURASIDONE HYDROCHLORIDE 80 mg/1 90 TABLET in 1 BOTTLE (65862-956-90)
65862-954-05 65862-954 HUMAN PRESCRIPTION DRUG LURASIDONE HYDROCHLORIDE LURASIDONE HYDROCHLORIDE TABLET ORAL 20230310 N/A ANDA ANDA208045 Aurobindo Pharma Limited LURASIDONE HYDROCHLORIDE 40 mg/1 500 TABLET in 1 BOTTLE (65862-954-05)
65862-954-30 65862-954 HUMAN PRESCRIPTION DRUG LURASIDONE HYDROCHLORIDE LURASIDONE HYDROCHLORIDE TABLET ORAL 20230310 N/A ANDA ANDA208045 Aurobindo Pharma Limited LURASIDONE HYDROCHLORIDE 40 mg/1 30 TABLET in 1 BOTTLE (65862-954-30)
65862-954-90 65862-954 HUMAN PRESCRIPTION DRUG LURASIDONE HYDROCHLORIDE LURASIDONE HYDROCHLORIDE TABLET ORAL 20230310 N/A ANDA ANDA208045 Aurobindo Pharma Limited LURASIDONE HYDROCHLORIDE 40 mg/1 90 TABLET in 1 BOTTLE (65862-954-90)
72189-598-30 72189-598 HUMAN PRESCRIPTION DRUG Lurasidone HCL Lurasidone HCL TABLET ORAL 20241216 N/A ANDA ANDA208045 Direct_rx LURASIDONE HYDROCHLORIDE 40 mg/1 30 TABLET in 1 BOTTLE (72189-598-30)
65862-953-05 65862-953 HUMAN PRESCRIPTION DRUG LURASIDONE HYDROCHLORIDE LURASIDONE HYDROCHLORIDE TABLET ORAL 20230310 N/A ANDA ANDA208045 Aurobindo Pharma Limited LURASIDONE HYDROCHLORIDE 20 mg/1 500 TABLET in 1 BOTTLE (65862-953-05)
65862-953-30 65862-953 HUMAN PRESCRIPTION DRUG LURASIDONE HYDROCHLORIDE LURASIDONE HYDROCHLORIDE TABLET ORAL 20230310 N/A ANDA ANDA208045 Aurobindo Pharma Limited LURASIDONE HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BOTTLE (65862-953-30)
65862-953-90 65862-953 HUMAN PRESCRIPTION DRUG LURASIDONE HYDROCHLORIDE LURASIDONE HYDROCHLORIDE TABLET ORAL 20230310 N/A ANDA ANDA208045 Aurobindo Pharma Limited LURASIDONE HYDROCHLORIDE 20 mg/1 90 TABLET in 1 BOTTLE (65862-953-90)
65862-957-05 65862-957 HUMAN PRESCRIPTION DRUG LURASIDONE HYDROCHLORIDE LURASIDONE HYDROCHLORIDE TABLET ORAL 20230310 N/A ANDA ANDA208045 Aurobindo Pharma Limited LURASIDONE HYDROCHLORIDE 120 mg/1 500 TABLET in 1 BOTTLE (65862-957-05)
65862-957-30 65862-957 HUMAN PRESCRIPTION DRUG LURASIDONE HYDROCHLORIDE LURASIDONE HYDROCHLORIDE TABLET ORAL 20230310 N/A ANDA ANDA208045 Aurobindo Pharma Limited LURASIDONE HYDROCHLORIDE 120 mg/1 30 TABLET in 1 BOTTLE (65862-957-30)
65862-957-90 65862-957 HUMAN PRESCRIPTION DRUG LURASIDONE HYDROCHLORIDE LURASIDONE HYDROCHLORIDE TABLET ORAL 20230310 N/A ANDA ANDA208045 Aurobindo Pharma Limited LURASIDONE HYDROCHLORIDE 120 mg/1 90 TABLET in 1 BOTTLE (65862-957-90)
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