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
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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
50090-2455-0 50090-2455 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20160812 N/A ANDA ANDA202633 A-S Medication Solutions PRAMIPEXOLE DIHYDROCHLORIDE .5 mg/1 30 TABLET in 1 BOTTLE (50090-2455-0)
50090-3280-0 50090-3280 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20171127 N/A ANDA ANDA202633 A-S Medication Solutions PRAMIPEXOLE DIHYDROCHLORIDE .25 mg/1 90 TABLET in 1 BOTTLE (50090-3280-0)
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)
65862-605-78 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)
57237-180-90 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 90 TABLET in 1 BOTTLE (57237-180-90)
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)
57237-181-99 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)
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)
65862-608-78 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)
65862-608-90 65862-608 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Aurobindo Pharma Limited PRAMIPEXOLE DIHYDROCHLORIDE 1 mg/1 90 TABLET in 1 BOTTLE (65862-608-90)
65862-608-99 65862-608 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20121026 N/A ANDA ANDA202633 Aurobindo Pharma Limited PRAMIPEXOLE DIHYDROCHLORIDE 1 mg/1 1000 TABLET in 1 BOTTLE (65862-608-99)
65862-609-78 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 10 BLISTER PACK in 1 CARTON (65862-609-78) / 10 TABLET in 1 BLISTER PACK (65862-609-10)
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)
65862-609-99 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 1000 TABLET in 1 BOTTLE (65862-609-99)
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