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=ANDA204994"
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
65862-747-03 65862-747 HUMAN PRESCRIPTION DRUG Lacosamide Lacosamide TABLET, FILM COATED ORAL 20230105 N/A ANDA ANDA204994 Aurobindo Pharma Limited LACOSAMIDE 50 mg/1 3 BLISTER PACK in 1 CARTON (65862-747-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-747-10)
65862-747-60 65862-747 HUMAN PRESCRIPTION DRUG Lacosamide Lacosamide TABLET, FILM COATED ORAL 20230105 N/A ANDA ANDA204994 Aurobindo Pharma Limited LACOSAMIDE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-747-60)
65862-749-03 65862-749 HUMAN PRESCRIPTION DRUG Lacosamide Lacosamide TABLET, FILM COATED ORAL 20230105 N/A ANDA ANDA204994 Aurobindo Pharma Limited LACOSAMIDE 150 mg/1 3 BLISTER PACK in 1 CARTON (65862-749-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-749-10)
65862-749-60 65862-749 HUMAN PRESCRIPTION DRUG Lacosamide Lacosamide TABLET, FILM COATED ORAL 20230105 N/A ANDA ANDA204994 Aurobindo Pharma Limited LACOSAMIDE 150 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-749-60)
65862-748-03 65862-748 HUMAN PRESCRIPTION DRUG Lacosamide Lacosamide TABLET, FILM COATED ORAL 20230105 N/A ANDA ANDA204994 Aurobindo Pharma Limited LACOSAMIDE 100 mg/1 3 BLISTER PACK in 1 CARTON (65862-748-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-748-10)
65862-748-60 65862-748 HUMAN PRESCRIPTION DRUG Lacosamide Lacosamide TABLET, FILM COATED ORAL 20230105 N/A ANDA ANDA204994 Aurobindo Pharma Limited LACOSAMIDE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-748-60)
65862-750-03 65862-750 HUMAN PRESCRIPTION DRUG Lacosamide Lacosamide TABLET, FILM COATED ORAL 20230105 N/A ANDA ANDA204994 Aurobindo Pharma Limited LACOSAMIDE 200 mg/1 3 BLISTER PACK in 1 CARTON (65862-750-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-750-10)
65862-750-60 65862-750 HUMAN PRESCRIPTION DRUG Lacosamide Lacosamide TABLET, FILM COATED ORAL 20230105 N/A ANDA ANDA204994 Aurobindo Pharma Limited LACOSAMIDE 200 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-750-60)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase