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=ANDA206402"
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
71335-2048-4 71335-2048 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20220322 N/A ANDA ANDA206402 Bryant Ranch Prepack GABAPENTIN 600 mg/1 120 TABLET in 1 BOTTLE (71335-2048-4)
71335-2281-1 71335-2281 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20231130 N/A ANDA ANDA206402 Bryant Ranch Prepack GABAPENTIN 600 mg/1 500 TABLET in 1 BOTTLE (71335-2281-1)
67877-428-38 67877-428 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20151101 N/A ANDA ANDA206402 Ascend Laboratories, LLC GABAPENTIN 600 mg/1 100 BLISTER PACK in 1 CARTON (67877-428-38) / 10 TABLET in 1 BLISTER PACK
67877-429-01 67877-429 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20151101 N/A ANDA ANDA206402 Ascend Laboratories, LLC GABAPENTIN 800 mg/1 100 TABLET in 1 BOTTLE (67877-429-01)
67877-429-05 67877-429 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20151101 N/A ANDA ANDA206402 Ascend Laboratories, LLC GABAPENTIN 800 mg/1 500 TABLET in 1 BOTTLE (67877-429-05)
67877-429-10 67877-429 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20151101 N/A ANDA ANDA206402 Ascend Laboratories, LLC GABAPENTIN 800 mg/1 1000 TABLET in 1 BOTTLE (67877-429-10)
67877-429-38 67877-429 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20151101 N/A ANDA ANDA206402 Ascend Laboratories, LLC GABAPENTIN 800 mg/1 100 BLISTER PACK in 1 CARTON (67877-429-38) / 10 TABLET in 1 BLISTER PACK
67877-428-01 67877-428 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20151101 N/A ANDA ANDA206402 Ascend Laboratories, LLC GABAPENTIN 600 mg/1 100 TABLET in 1 BOTTLE (67877-428-01)
67877-428-05 67877-428 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20151101 N/A ANDA ANDA206402 Ascend Laboratories, LLC GABAPENTIN 600 mg/1 500 TABLET in 1 BOTTLE (67877-428-05)
67877-428-10 67877-428 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20151101 N/A ANDA ANDA206402 Ascend Laboratories, LLC GABAPENTIN 600 mg/1 1000 TABLET in 1 BOTTLE (67877-428-10)
50090-2539-0 50090-2539 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20161024 N/A ANDA ANDA206402 A-S Medication Solutions GABAPENTIN 600 mg/1 90 TABLET in 1 BOTTLE (50090-2539-0)
50090-2539-1 50090-2539 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20170216 N/A ANDA ANDA206402 A-S Medication Solutions GABAPENTIN 600 mg/1 60 TABLET in 1 BOTTLE (50090-2539-1)
50090-2539-2 50090-2539 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20161019 N/A ANDA ANDA206402 A-S Medication Solutions GABAPENTIN 600 mg/1 30 TABLET in 1 BOTTLE (50090-2539-2)
70518-2912-0 70518-2912 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20201020 N/A ANDA ANDA206402 REMEDYREPACK INC. GABAPENTIN 800 mg/1 100 POUCH in 1 BOX (70518-2912-0) / 1 TABLET in 1 POUCH (70518-2912-1)
80425-0035-1 80425-0035 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20151101 N/A ANDA ANDA206402 Advanced Rx Pharmacy of Tennessee, LLC GABAPENTIN 800 mg/1 30 TABLET in 1 BOTTLE (80425-0035-1)
70518-2842-1 70518-2842 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20210805 N/A ANDA ANDA206402 REMEDYREPACK INC. GABAPENTIN 600 mg/1 100 POUCH in 1 BOX (70518-2842-1) / 1 TABLET in 1 POUCH (70518-2842-2)
71335-1200-1 71335-1200 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20190506 N/A ANDA ANDA206402 Bryant Ranch Prepack GABAPENTIN 600 mg/1 30 TABLET in 1 BOTTLE (71335-1200-1)
71335-1200-4 71335-1200 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20190422 N/A ANDA ANDA206402 Bryant Ranch Prepack GABAPENTIN 600 mg/1 90 TABLET in 1 BOTTLE (71335-1200-4)
71335-1200-5 71335-1200 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20220923 N/A ANDA ANDA206402 Bryant Ranch Prepack GABAPENTIN 600 mg/1 100 TABLET in 1 BOTTLE (71335-1200-5)
71335-1200-6 71335-1200 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20190502 N/A ANDA ANDA206402 Bryant Ranch Prepack GABAPENTIN 600 mg/1 120 TABLET in 1 BOTTLE (71335-1200-6)
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