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=ANDA208180"
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
42571-259-05 42571-259 HUMAN PRESCRIPTION DRUG ROFLUMILAST Roflumilast TABLET ORAL 20221019 N/A ANDA ANDA208180 Micro Labs Limited ROFLUMILAST 500 ug/1 500 TABLET in 1 BOTTLE (42571-259-05)
42571-259-17 42571-259 HUMAN PRESCRIPTION DRUG ROFLUMILAST Roflumilast TABLET ORAL 20221019 N/A ANDA ANDA208180 Micro Labs Limited ROFLUMILAST 500 ug/1 11 BLISTER PACK in 1 CARTON (42571-259-17) / 10 TABLET in 1 BLISTER PACK (42571-259-32)
42571-259-30 42571-259 HUMAN PRESCRIPTION DRUG ROFLUMILAST Roflumilast TABLET ORAL 20221019 N/A ANDA ANDA208180 Micro Labs Limited ROFLUMILAST 500 ug/1 30 TABLET in 1 BOTTLE (42571-259-30)
42571-259-90 42571-259 HUMAN PRESCRIPTION DRUG ROFLUMILAST Roflumilast TABLET ORAL 20221019 N/A ANDA ANDA208180 Micro Labs Limited ROFLUMILAST 500 ug/1 90 TABLET in 1 BOTTLE (42571-259-90)
42571-369-05 42571-369 HUMAN PRESCRIPTION DRUG ROFLUMILAST ROFLUMILAST TABLET ORAL 20230501 N/A ANDA ANDA208180 Micro Labs Limited ROFLUMILAST 250 ug/1 500 TABLET in 1 BOTTLE (42571-369-05)
42571-369-11 42571-369 HUMAN PRESCRIPTION DRUG ROFLUMILAST ROFLUMILAST TABLET ORAL 20230501 N/A ANDA ANDA208180 Micro Labs Limited ROFLUMILAST 250 ug/1 10 BLISTER PACK in 1 CARTON (42571-369-11) / 10 TABLET in 1 BLISTER PACK (42571-369-32)
42571-369-30 42571-369 HUMAN PRESCRIPTION DRUG ROFLUMILAST ROFLUMILAST TABLET ORAL 20230501 N/A ANDA ANDA208180 Micro Labs Limited ROFLUMILAST 250 ug/1 30 TABLET in 1 BOTTLE (42571-369-30)
42571-369-83 42571-369 HUMAN PRESCRIPTION DRUG ROFLUMILAST ROFLUMILAST TABLET ORAL 20230501 N/A ANDA ANDA208180 Micro Labs Limited ROFLUMILAST 250 ug/1 28 TABLET in 1 BOTTLE (42571-369-83)
42571-369-90 42571-369 HUMAN PRESCRIPTION DRUG ROFLUMILAST ROFLUMILAST TABLET ORAL 20230501 N/A ANDA ANDA208180 Micro Labs Limited ROFLUMILAST 250 ug/1 90 TABLET in 1 BOTTLE (42571-369-90)
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