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=ANDA077662"
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
63629-7307-4 63629-7307 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20180807 N/A ANDA ANDA077662 Bryant Ranch Prepack GABAPENTIN 600 mg/1 120 TABLET in 1 BOTTLE (63629-7307-4)
63629-7307-5 63629-7307 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20181107 N/A ANDA ANDA077662 Bryant Ranch Prepack GABAPENTIN 600 mg/1 60 TABLET in 1 BOTTLE (63629-7307-5)
63629-7307-6 63629-7307 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20241008 N/A ANDA ANDA077662 Bryant Ranch Prepack GABAPENTIN 600 mg/1 30 TABLET in 1 BOTTLE (63629-7307-6)
63629-7307-3 63629-7307 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20180730 N/A ANDA ANDA077662 Bryant Ranch Prepack GABAPENTIN 600 mg/1 100 TABLET in 1 BOTTLE (63629-7307-3)
63629-7307-2 63629-7307 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20241008 N/A ANDA ANDA077662 Bryant Ranch Prepack GABAPENTIN 600 mg/1 58 TABLET in 1 BOTTLE (63629-7307-2)
63629-7307-1 63629-7307 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20170630 N/A ANDA ANDA077662 Bryant Ranch Prepack GABAPENTIN 600 mg/1 90 TABLET in 1 BOTTLE (63629-7307-1)
63187-010-30 63187-010 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20161201 N/A ANDA ANDA077662 Proficient Rx LP GABAPENTIN 800 mg/1 30 TABLET in 1 BOTTLE (63187-010-30)
63187-010-60 63187-010 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20140401 N/A ANDA ANDA077662 Proficient Rx LP GABAPENTIN 800 mg/1 60 TABLET in 1 BOTTLE (63187-010-60)
63187-010-90 63187-010 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20140401 N/A ANDA ANDA077662 Proficient Rx LP GABAPENTIN 800 mg/1 90 TABLET in 1 BOTTLE (63187-010-90)
63187-057-30 63187-057 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20140601 N/A ANDA ANDA077662 Proficient Rx LP GABAPENTIN 600 mg/1 30 TABLET in 1 BOTTLE (63187-057-30)
63187-057-60 63187-057 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20140602 N/A ANDA ANDA077662 Proficient Rx LP GABAPENTIN 600 mg/1 60 TABLET in 1 BOTTLE (63187-057-60)
63187-057-90 63187-057 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20140602 N/A ANDA ANDA077662 Proficient Rx LP GABAPENTIN 600 mg/1 90 TABLET in 1 BOTTLE (63187-057-90)
63187-057-00 63187-057 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20140602 N/A ANDA ANDA077662 Proficient Rx LP GABAPENTIN 600 mg/1 100 TABLET in 1 BOTTLE (63187-057-00)
55289-959-30 55289-959 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20200127 N/A ANDA ANDA077662 PD-Rx Pharmaceuticals, Inc. GABAPENTIN 600 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (55289-959-30)
55289-959-60 55289-959 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20111010 N/A ANDA ANDA077662 PD-Rx Pharmaceuticals, Inc. GABAPENTIN 600 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (55289-959-60)
55289-959-90 55289-959 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20111010 N/A ANDA ANDA077662 PD-Rx Pharmaceuticals, Inc. GABAPENTIN 600 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (55289-959-90)
55289-959-98 55289-959 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20111010 N/A ANDA ANDA077662 PD-Rx Pharmaceuticals, Inc. GABAPENTIN 600 mg/1 120 TABLET in 1 BOTTLE, PLASTIC (55289-959-98)
68001-411-00 68001-411 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20190930 N/A ANDA ANDA077662 BluePoint Laboratories GABAPENTIN 600 mg/1 100 TABLET in 1 BOTTLE (68001-411-00)
68001-411-03 68001-411 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20190930 N/A ANDA ANDA077662 BluePoint Laboratories GABAPENTIN 600 mg/1 500 TABLET in 1 BOTTLE (68001-411-03)
68001-412-00 68001-412 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20190930 N/A ANDA ANDA077662 BluePoint Laboratories GABAPENTIN 800 mg/1 100 TABLET in 1 BOTTLE (68001-412-00)
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