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=ANDA202164"
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
33342-033-06 33342-033 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE .5 mg/1 30 BLISTER PACK in 1 CARTON (33342-033-06) / 1 TABLET in 1 BLISTER PACK
33342-033-10 33342-033 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE .5 mg/1 90 TABLET in 1 BOTTLE (33342-033-10)
33342-033-12 33342-033 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE .5 mg/1 100 BLISTER PACK in 1 CARTON (33342-033-12) / 1 TABLET in 1 BLISTER PACK
33342-033-15 33342-033 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE .5 mg/1 500 TABLET in 1 BOTTLE (33342-033-15)
33342-034-06 33342-034 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE 1 mg/1 30 BLISTER PACK in 1 CARTON (33342-034-06) / 1 TABLET in 1 BLISTER PACK
33342-034-10 33342-034 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE 1 mg/1 90 TABLET in 1 BOTTLE (33342-034-10)
33342-034-12 33342-034 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE 1 mg/1 100 BLISTER PACK in 1 CARTON (33342-034-12) / 1 TABLET in 1 BLISTER PACK
33342-034-15 33342-034 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE 1 mg/1 500 TABLET in 1 BOTTLE (33342-034-15)
33342-032-06 33342-032 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE .25 mg/1 30 BLISTER PACK in 1 CARTON (33342-032-06) / 1 TABLET in 1 BLISTER PACK
33342-032-10 33342-032 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE .25 mg/1 90 TABLET in 1 BOTTLE (33342-032-10)
33342-032-12 33342-032 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE .25 mg/1 100 BLISTER PACK in 1 CARTON (33342-032-12) / 1 TABLET in 1 BLISTER PACK
33342-032-15 33342-032 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE .25 mg/1 500 TABLET in 1 BOTTLE (33342-032-15)
33342-031-06 33342-031 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1 30 BLISTER PACK in 1 CARTON (33342-031-06) / 1 TABLET in 1 BLISTER PACK
33342-031-10 33342-031 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1 90 TABLET in 1 BOTTLE (33342-031-10)
33342-031-12 33342-031 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1 100 BLISTER PACK in 1 CARTON (33342-031-12) / 1 TABLET in 1 BLISTER PACK
33342-031-15 33342-031 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1 500 TABLET in 1 BOTTLE (33342-031-15)
33342-035-06 33342-035 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE 1.5 mg/1 30 BLISTER PACK in 1 CARTON (33342-035-06) / 1 TABLET in 1 BLISTER PACK
33342-035-10 33342-035 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE 1.5 mg/1 90 TABLET in 1 BOTTLE (33342-035-10)
33342-035-12 33342-035 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE 1.5 mg/1 100 BLISTER PACK in 1 CARTON (33342-035-12) / 1 TABLET in 1 BLISTER PACK
33342-035-15 33342-035 HUMAN PRESCRIPTION DRUG Pramipexole dihydrochloride Pramipexole dihydrochloride TABLET ORAL 20120921 N/A ANDA ANDA202164 Macleods Pharmaceuticals Limited PRAMIPEXOLE DIHYDROCHLORIDE 1.5 mg/1 500 TABLET in 1 BOTTLE (33342-035-15)
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