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=ANDA077633"
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
0615-8267-39 0615-8267 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20190109 N/A ANDA ANDA077633 NCS HealthCare of KY, LLC dba Vangard Labs LAMOTRIGINE 200 mg/1 30 TABLET in 1 BLISTER PACK (0615-8267-39)
16714-194-01 16714-194 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20211117 N/A ANDA ANDA077633 Northstar Rx LLC. LAMOTRIGINE 25 mg/1 100 TABLET in 1 BOTTLE (16714-194-01)
16714-195-01 16714-195 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20211117 N/A ANDA ANDA077633 Northstar Rx LLC. LAMOTRIGINE 100 mg/1 100 TABLET in 1 BOTTLE (16714-195-01)
16714-196-01 16714-196 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20211117 N/A ANDA ANDA077633 Northstar Rx LLC. LAMOTRIGINE 150 mg/1 60 TABLET in 1 BOTTLE (16714-196-01)
16714-197-01 16714-197 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20211117 N/A ANDA ANDA077633 Northstar Rx LLC. LAMOTRIGINE 200 mg/1 60 TABLET in 1 BOTTLE (16714-197-01)
50090-5827-0 50090-5827 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20211026 N/A ANDA ANDA077633 A-S Medication Solutions LAMOTRIGINE 100 mg/1 30 TABLET in 1 BOTTLE (50090-5827-0)
50090-5850-1 50090-5850 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20211108 N/A ANDA ANDA077633 A-S Medication Solutions LAMOTRIGINE 150 mg/1 30 TABLET in 1 BOTTLE (50090-5850-1)
50090-5827-1 50090-5827 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20211026 N/A ANDA ANDA077633 A-S Medication Solutions LAMOTRIGINE 100 mg/1 60 TABLET in 1 BOTTLE (50090-5827-1)
50090-5827-2 50090-5827 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20211026 N/A ANDA ANDA077633 A-S Medication Solutions LAMOTRIGINE 100 mg/1 90 TABLET in 1 BOTTLE (50090-5827-2)
50090-5850-0 50090-5850 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20211108 N/A ANDA ANDA077633 A-S Medication Solutions LAMOTRIGINE 150 mg/1 60 TABLET in 1 BOTTLE (50090-5850-0)
65841-682-01 65841-682 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20090127 N/A ANDA ANDA077633 Zydus Lifesciences Limited LAMOTRIGINE 25 mg/1 100 TABLET in 1 BOTTLE (65841-682-01)
65841-682-16 65841-682 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20090127 N/A ANDA ANDA077633 Zydus Lifesciences Limited LAMOTRIGINE 25 mg/1 90 TABLET in 1 BOTTLE (65841-682-16)
65841-683-01 65841-683 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20090127 N/A ANDA ANDA077633 Zydus Lifesciences Limited LAMOTRIGINE 50 mg/1 100 TABLET in 1 BOTTLE (65841-683-01)
65841-683-05 65841-683 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20090127 N/A ANDA ANDA077633 Zydus Lifesciences Limited LAMOTRIGINE 50 mg/1 500 TABLET in 1 BOTTLE (65841-683-05)
65841-683-10 65841-683 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20090127 N/A ANDA ANDA077633 Zydus Lifesciences Limited LAMOTRIGINE 50 mg/1 1000 TABLET in 1 BOTTLE (65841-683-10)
65841-683-16 65841-683 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20090127 N/A ANDA ANDA077633 Zydus Lifesciences Limited LAMOTRIGINE 50 mg/1 90 TABLET in 1 BOTTLE (65841-683-16)
65841-684-01 65841-684 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20090127 N/A ANDA ANDA077633 Zydus Lifesciences Limited LAMOTRIGINE 100 mg/1 100 TABLET in 1 BOTTLE (65841-684-01)
65841-684-05 65841-684 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20090127 N/A ANDA ANDA077633 Zydus Lifesciences Limited LAMOTRIGINE 100 mg/1 500 TABLET in 1 BOTTLE (65841-684-05)
65841-684-10 65841-684 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20090127 N/A ANDA ANDA077633 Zydus Lifesciences Limited LAMOTRIGINE 100 mg/1 1000 TABLET in 1 BOTTLE (65841-684-10)
65841-684-16 65841-684 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20090127 N/A ANDA ANDA077633 Zydus Lifesciences Limited LAMOTRIGINE 100 mg/1 90 TABLET in 1 BOTTLE (65841-684-16)
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