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
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)
82619-145-01 82619-145 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20240901 N/A ANDA ANDA205101 Creekwood Pharmaceuticals LLC GABAPENTIN 600 mg/1 100 TABLET in 1 BOTTLE (82619-145-01)
82619-145-02 82619-145 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20240901 N/A ANDA ANDA205101 Creekwood Pharmaceuticals LLC GABAPENTIN 600 mg/1 500 TABLET in 1 BOTTLE (82619-145-02)
68788-7757-1 68788-7757 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20200701 N/A ANDA ANDA205101 Preferred Pharmaceuticals, Inc. GABAPENTIN 800 mg/1 100 TABLET in 1 BOTTLE (68788-7757-1)
68788-7757-3 68788-7757 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20200701 N/A ANDA ANDA205101 Preferred Pharmaceuticals, Inc. GABAPENTIN 800 mg/1 30 TABLET in 1 BOTTLE (68788-7757-3)
68788-7757-6 68788-7757 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20200701 N/A ANDA ANDA205101 Preferred Pharmaceuticals, Inc. GABAPENTIN 800 mg/1 60 TABLET in 1 BOTTLE (68788-7757-6)
68788-7757-8 68788-7757 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20200701 N/A ANDA ANDA205101 Preferred Pharmaceuticals, Inc. GABAPENTIN 800 mg/1 120 TABLET in 1 BOTTLE (68788-7757-8)
68788-7757-9 68788-7757 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20200701 N/A ANDA ANDA205101 Preferred Pharmaceuticals, Inc. GABAPENTIN 800 mg/1 90 TABLET in 1 BOTTLE (68788-7757-9)
71205-774-30 71205-774 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20230314 N/A ANDA ANDA205101 Proficient Rx LP GABAPENTIN 800 mg/1 30 TABLET in 1 BOTTLE (71205-774-30)
72189-178-30 72189-178 HUMAN PRESCRIPTION DRUG GABAPENTIN GABAPENTIN TABLET ORAL 20210208 N/A ANDA ANDA205101 DIRECT RX GABAPENTIN 800 mg/1 30 TABLET in 1 BOTTLE (72189-178-30)
72189-178-72 72189-178 HUMAN PRESCRIPTION DRUG GABAPENTIN GABAPENTIN TABLET ORAL 20210208 N/A ANDA ANDA205101 DIRECT RX GABAPENTIN 800 mg/1 120 TABLET in 1 BOTTLE (72189-178-72)
72189-178-90 72189-178 HUMAN PRESCRIPTION DRUG GABAPENTIN GABAPENTIN TABLET ORAL 20210208 N/A ANDA ANDA205101 DIRECT RX GABAPENTIN 800 mg/1 90 TABLET in 1 BOTTLE (72189-178-90)
60760-517-30 60760-517 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20251212 N/A ANDA ANDA205101 St. Mary's Medical Park Pharmacy GABAPENTIN 800 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (60760-517-30)
60760-517-90 60760-517 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20251212 N/A ANDA ANDA205101 St. Mary's Medical Park Pharmacy GABAPENTIN 800 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (60760-517-90)
77771-177-05 77771-177 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20231103 N/A ANDA ANDA205101 Radha Pharmaceuticals, Inc. GABAPENTIN 600 mg/1 500 TABLET in 1 BOTTLE (77771-177-05)
77771-177-90 77771-177 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20231103 N/A ANDA ANDA205101 Radha Pharmaceuticals, Inc. GABAPENTIN 600 mg/1 90 TABLET in 1 BOTTLE (77771-177-90)
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)
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