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
67046-1536-3 67046-1536 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20250325 N/A ANDA ANDA205101 Coupler LLC GABAPENTIN 800 mg/1 30 TABLET in 1 BLISTER PACK (67046-1536-3)
72189-313-60 72189-313 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20220117 N/A ANDA ANDA205101 Directrx GABAPENTIN 600 mg/1 60 TABLET in 1 BOTTLE (72189-313-60)
72189-313-72 72189-313 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20220117 N/A ANDA ANDA205101 Directrx GABAPENTIN 600 mg/1 120 TABLET in 1 BOTTLE (72189-313-72)
72189-313-90 72189-313 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20220117 N/A ANDA ANDA205101 Directrx GABAPENTIN 600 mg/1 90 TABLET in 1 BOTTLE (72189-313-90)
76420-497-01 76420-497 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20221010 N/A ANDA ANDA205101 Asclemed USA, Inc. GABAPENTIN 800 mg/1 100 TABLET in 1 BOTTLE (76420-497-01)
76420-497-05 76420-497 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20221010 N/A ANDA ANDA205101 Asclemed USA, Inc. GABAPENTIN 800 mg/1 500 TABLET in 1 BOTTLE (76420-497-05)
76420-497-12 76420-497 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20221010 N/A ANDA ANDA205101 Asclemed USA, Inc. GABAPENTIN 800 mg/1 120 TABLET in 1 BOTTLE (76420-497-12)
76420-497-24 76420-497 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20221010 N/A ANDA ANDA205101 Asclemed USA, Inc. GABAPENTIN 800 mg/1 240 TABLET in 1 BOTTLE (76420-497-24)
76420-497-30 76420-497 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20221010 N/A ANDA ANDA205101 Asclemed USA, Inc. GABAPENTIN 800 mg/1 30 TABLET in 1 BOTTLE (76420-497-30)
76420-497-60 76420-497 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20221010 N/A ANDA ANDA205101 Asclemed USA, Inc. GABAPENTIN 800 mg/1 60 TABLET in 1 BOTTLE (76420-497-60)
76420-497-90 76420-497 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20221010 N/A ANDA ANDA205101 Asclemed USA, Inc. GABAPENTIN 800 mg/1 90 TABLET in 1 BOTTLE (76420-497-90)
72162-1530-1 72162-1530 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20240202 N/A ANDA ANDA205101 Bryant Ranch Prepack GABAPENTIN 600 mg/1 100 TABLET in 1 BOTTLE (72162-1530-1)
72162-1530-5 72162-1530 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20240202 N/A ANDA ANDA205101 Bryant Ranch Prepack GABAPENTIN 600 mg/1 500 TABLET in 1 BOTTLE (72162-1530-5)
63629-8490-1 63629-8490 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20180820 N/A ANDA ANDA205101 Bryant Ranch Prepack GABAPENTIN 800 mg/1 100 TABLET in 1 BOTTLE (63629-8490-1)
82619-146-01 82619-146 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20240901 N/A ANDA ANDA205101 Creekwood Pharmaceuticals LLC GABAPENTIN 800 mg/1 100 TABLET in 1 BOTTLE (82619-146-01)
82619-146-02 82619-146 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20240901 N/A ANDA ANDA205101 Creekwood Pharmaceuticals LLC GABAPENTIN 800 mg/1 500 TABLET in 1 BOTTLE (82619-146-02)
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)
68788-7847-1 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)
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