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=ANDA090383"
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
42571-080-05 42571-080 HUMAN PRESCRIPTION DRUG Simvastatin Simvastatin TABLET ORAL 20130613 N/A ANDA ANDA090383 Micro Labs Limited SIMVASTATIN 80 mg/1 500 TABLET in 1 BOTTLE (42571-080-05)
42571-080-10 42571-080 HUMAN PRESCRIPTION DRUG Simvastatin Simvastatin TABLET ORAL 20130613 N/A ANDA ANDA090383 Micro Labs Limited SIMVASTATIN 80 mg/1 1000 TABLET in 1 BOTTLE (42571-080-10)
42571-080-30 42571-080 HUMAN PRESCRIPTION DRUG Simvastatin Simvastatin TABLET ORAL 20130613 N/A ANDA ANDA090383 Micro Labs Limited SIMVASTATIN 80 mg/1 30 TABLET in 1 BOTTLE (42571-080-30)
42571-080-60 42571-080 HUMAN PRESCRIPTION DRUG Simvastatin Simvastatin TABLET ORAL 20130613 N/A ANDA ANDA090383 Micro Labs Limited SIMVASTATIN 80 mg/1 60 TABLET in 1 BOTTLE (42571-080-60)
42571-080-90 42571-080 HUMAN PRESCRIPTION DRUG Simvastatin Simvastatin TABLET ORAL 20130613 N/A ANDA ANDA090383 Micro Labs Limited SIMVASTATIN 80 mg/1 90 TABLET in 1 BOTTLE (42571-080-90)
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