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=ANDA205101"
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
68788-7774-6 68788-7774 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20200824 N/A ANDA ANDA205101 Preferred Pharmaceuticals, Inc. GABAPENTIN 800 mg/1 60 TABLET in 1 BOTTLE (68788-7774-6)
68788-7774-8 68788-7774 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20200824 N/A ANDA ANDA205101 Preferred Pharmaceuticals, Inc. GABAPENTIN 800 mg/1 120 TABLET in 1 BOTTLE (68788-7774-8)
68788-7774-9 68788-7774 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20200824 N/A ANDA ANDA205101 Preferred Pharmaceuticals, Inc. GABAPENTIN 800 mg/1 90 TABLET in 1 BOTTLE (68788-7774-9)
50228-177-01 50228-177 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20180820 N/A ANDA ANDA205101 ScieGen Pharmaceuticals, Inc. GABAPENTIN 600 mg/1 100 TABLET in 1 BOTTLE (50228-177-01)
50228-177-05 50228-177 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20160204 N/A ANDA ANDA205101 ScieGen Pharmaceuticals, Inc. GABAPENTIN 600 mg/1 500 TABLET in 1 BOTTLE (50228-177-05)
50228-177-30 50228-177 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20160204 N/A ANDA ANDA205101 ScieGen Pharmaceuticals, Inc. GABAPENTIN 600 mg/1 30 TABLET in 1 BOTTLE (50228-177-30)
50228-178-01 50228-178 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20180820 N/A ANDA ANDA205101 ScieGen Pharmaceuticals, Inc. GABAPENTIN 800 mg/1 100 TABLET in 1 BOTTLE (50228-178-01)
50228-178-05 50228-178 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20160204 N/A ANDA ANDA205101 ScieGen Pharmaceuticals, Inc. GABAPENTIN 800 mg/1 500 TABLET in 1 BOTTLE (50228-178-05)
50228-178-30 50228-178 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20160204 N/A ANDA ANDA205101 ScieGen Pharmaceuticals, Inc. GABAPENTIN 800 mg/1 30 TABLET in 1 BOTTLE (50228-178-30)
68071-2206-1 68071-2206 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20200706 N/A ANDA ANDA205101 NuCare Pharmaceuticals,Inc. GABAPENTIN 800 mg/1 100 TABLET in 1 BOTTLE (68071-2206-1)
68071-2214-9 68071-2214 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20200708 N/A ANDA ANDA205101 NuCare Pharmaceuticals,Inc. GABAPENTIN 800 mg/1 90 TABLET in 1 BOTTLE (68071-2214-9)
68788-7840-1 68788-7840 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20210118 N/A ANDA ANDA205101 Preferred Pharmaceuticals, Inc. GABAPENTIN 600 mg/1 100 TABLET in 1 BOTTLE (68788-7840-1)
68788-7840-3 68788-7840 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20210118 N/A ANDA ANDA205101 Preferred Pharmaceuticals, Inc. GABAPENTIN 600 mg/1 30 TABLET in 1 BOTTLE (68788-7840-3)
68788-7840-6 68788-7840 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20210118 N/A ANDA ANDA205101 Preferred Pharmaceuticals, Inc. GABAPENTIN 600 mg/1 60 TABLET in 1 BOTTLE (68788-7840-6)
68788-7840-8 68788-7840 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20210118 N/A ANDA ANDA205101 Preferred Pharmaceuticals, Inc. GABAPENTIN 600 mg/1 120 TABLET in 1 BOTTLE (68788-7840-8)
68788-7840-9 68788-7840 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20210118 N/A ANDA ANDA205101 Preferred Pharmaceuticals, Inc. GABAPENTIN 600 mg/1 90 TABLET in 1 BOTTLE (68788-7840-9)
68788-7847-1 68788-7847 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20210121 N/A ANDA ANDA205101 Preferred Pharmaceuticals Inc. GABAPENTIN 600 mg/1 100 TABLET in 1 BOTTLE (68788-7847-1)
68788-7847-3 68788-7847 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20210121 N/A ANDA ANDA205101 Preferred Pharmaceuticals Inc. GABAPENTIN 600 mg/1 30 TABLET in 1 BOTTLE (68788-7847-3)
68788-7847-6 68788-7847 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20210121 N/A ANDA ANDA205101 Preferred Pharmaceuticals Inc. GABAPENTIN 600 mg/1 60 TABLET in 1 BOTTLE (68788-7847-6)
68788-7847-8 68788-7847 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20210121 N/A ANDA ANDA205101 Preferred Pharmaceuticals Inc. GABAPENTIN 600 mg/1 120 TABLET in 1 BOTTLE (68788-7847-8)
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