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=ANDA202633"
符合检索条件的记录共 44 条，共 3 页，当前第 2 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
57237-184-99 57237-184 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Rising Pharma Holdings, Inc. PRAMIPEXOLE DIHYDROCHLORIDE 1 mg/1 1000 TABLET in 1 BOTTLE (57237-184-99)
57237-185-90 57237-185 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Rising Pharma Holdings, Inc. PRAMIPEXOLE DIHYDROCHLORIDE 1.5 mg/1 90 TABLET in 1 BOTTLE (57237-185-90)
57237-180-99 57237-180 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Rising Pharma Holdings, Inc. PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1 1000 TABLET in 1 BOTTLE (57237-180-99)
57237-181-99 57237-181 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Rising Pharma Holdings, Inc. PRAMIPEXOLE DIHYDROCHLORIDE .25 mg/1 1000 TABLET in 1 BOTTLE (57237-181-99)
57237-181-90 57237-181 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Rising Pharma Holdings, Inc. PRAMIPEXOLE DIHYDROCHLORIDE .25 mg/1 90 TABLET in 1 BOTTLE (57237-181-90)
57237-185-99 57237-185 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Rising Pharma Holdings, Inc. PRAMIPEXOLE DIHYDROCHLORIDE 1.5 mg/1 1000 TABLET in 1 BOTTLE (57237-185-99)
65862-605-78 65862-605 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Aurobindo Pharma Limited PRAMIPEXOLE DIHYDROCHLORIDE .25 mg/1 10 BLISTER PACK in 1 CARTON (65862-605-78) / 10 TABLET in 1 BLISTER PACK (65862-605-10)
65862-605-90 65862-605 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Aurobindo Pharma Limited PRAMIPEXOLE DIHYDROCHLORIDE .25 mg/1 90 TABLET in 1 BOTTLE (65862-605-90)
65862-605-99 65862-605 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Aurobindo Pharma Limited PRAMIPEXOLE DIHYDROCHLORIDE .25 mg/1 1000 TABLET in 1 BOTTLE (65862-605-99)
65862-606-78 65862-606 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Aurobindo Pharma Limited PRAMIPEXOLE DIHYDROCHLORIDE .5 mg/1 10 BLISTER PACK in 1 CARTON (65862-606-78) / 10 TABLET in 1 BLISTER PACK (65862-606-10)
65862-606-90 65862-606 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Aurobindo Pharma Limited PRAMIPEXOLE DIHYDROCHLORIDE .5 mg/1 90 TABLET in 1 BOTTLE (65862-606-90)
65862-606-99 65862-606 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Aurobindo Pharma Limited PRAMIPEXOLE DIHYDROCHLORIDE .5 mg/1 1000 TABLET in 1 BOTTLE (65862-606-99)
65862-607-78 65862-607 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Aurobindo Pharma Limited PRAMIPEXOLE DIHYDROCHLORIDE .75 mg/1 10 BLISTER PACK in 1 CARTON (65862-607-78) / 10 TABLET in 1 BLISTER PACK (65862-607-10)
65862-607-90 65862-607 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Aurobindo Pharma Limited PRAMIPEXOLE DIHYDROCHLORIDE .75 mg/1 90 TABLET in 1 BOTTLE (65862-607-90)
65862-607-99 65862-607 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Aurobindo Pharma Limited PRAMIPEXOLE DIHYDROCHLORIDE .75 mg/1 1000 TABLET in 1 BOTTLE (65862-607-99)
65862-604-78 65862-604 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Aurobindo Pharma Limited PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1 10 BLISTER PACK in 1 CARTON (65862-604-78) / 10 TABLET in 1 BLISTER PACK (65862-604-10)
65862-604-90 65862-604 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Aurobindo Pharma Limited PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1 90 TABLET in 1 BOTTLE (65862-604-90)
65862-604-99 65862-604 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Aurobindo Pharma Limited PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1 1000 TABLET in 1 BOTTLE (65862-604-99)
65862-608-78 65862-608 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Aurobindo Pharma Limited PRAMIPEXOLE DIHYDROCHLORIDE 1 mg/1 10 BLISTER PACK in 1 CARTON (65862-608-78) / 10 TABLET in 1 BLISTER PACK (65862-608-10)
65862-609-90 65862-609 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Aurobindo Pharma Limited PRAMIPEXOLE DIHYDROCHLORIDE 1.5 mg/1 90 TABLET in 1 BOTTLE (65862-609-90)
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