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=ANDA207004"
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
42571-221-05 42571-221 HUMAN PRESCRIPTION DRUG RASAGILINE Rasagiline TABLET ORAL 20190403 N/A ANDA ANDA207004 Micro Labs Limited RASAGILINE MESYLATE 1 mg/1 500 TABLET in 1 BOTTLE (42571-221-05)
42571-221-10 42571-221 HUMAN PRESCRIPTION DRUG RASAGILINE Rasagiline TABLET ORAL 20190403 N/A ANDA ANDA207004 Micro Labs Limited RASAGILINE MESYLATE 1 mg/1 1000 TABLET in 1 BOTTLE (42571-221-10)
42571-221-30 42571-221 HUMAN PRESCRIPTION DRUG RASAGILINE Rasagiline TABLET ORAL 20190403 N/A ANDA ANDA207004 Micro Labs Limited RASAGILINE MESYLATE 1 mg/1 30 TABLET in 1 BOTTLE (42571-221-30)
42571-220-30 42571-220 HUMAN PRESCRIPTION DRUG RASAGILINE Rasagiline TABLET ORAL 20190403 N/A ANDA ANDA207004 Micro Labs Limited RASAGILINE MESYLATE .5 mg/1 30 TABLET in 1 BOTTLE (42571-220-30)
42571-220-10 42571-220 HUMAN PRESCRIPTION DRUG RASAGILINE Rasagiline TABLET ORAL 20190403 N/A ANDA ANDA207004 Micro Labs Limited RASAGILINE MESYLATE .5 mg/1 1000 TABLET in 1 BOTTLE (42571-220-10)
42571-220-05 42571-220 HUMAN PRESCRIPTION DRUG RASAGILINE Rasagiline TABLET ORAL 20190403 N/A ANDA ANDA207004 Micro Labs Limited RASAGILINE MESYLATE .5 mg/1 500 TABLET in 1 BOTTLE (42571-220-05)
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