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
68788-7847-9 68788-7847 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20210121 N/A ANDA ANDA205101 Preferred Pharmaceuticals Inc. GABAPENTIN 600 mg/1 90 TABLET in 1 BOTTLE (68788-7847-9)
60760-743-90 60760-743 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20210128 N/A ANDA ANDA205101 St. Mary's Medical Park Pharmacy GABAPENTIN 600 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (60760-743-90)
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)
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)
63629-8489-1 63629-8489 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20160204 N/A ANDA ANDA205101 Bryant Ranch Prepack GABAPENTIN 800 mg/1 500 TABLET in 1 BOTTLE (63629-8489-1)
63629-8491-1 63629-8491 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20160204 N/A ANDA ANDA205101 Bryant Ranch Prepack GABAPENTIN 600 mg/1 500 TABLET in 1 BOTTLE (63629-8491-1)
63629-8492-1 63629-8492 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20180820 N/A ANDA ANDA205101 Bryant Ranch Prepack GABAPENTIN 600 mg/1 100 TABLET in 1 BOTTLE (63629-8492-1)
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)
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)
72189-313-90 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)
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)
72189-313-72 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)
72189-313-60 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)
76420-235-30 76420-235 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20220707 N/A ANDA ANDA205101 Asclemed USA, Inc. GABAPENTIN 600 mg/1 30 TABLET in 1 BOTTLE (76420-235-30)
76420-235-90 76420-235 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20220707 N/A ANDA ANDA205101 Asclemed USA, Inc. GABAPENTIN 600 mg/1 90 TABLET in 1 BOTTLE (76420-235-90)
76420-235-12 76420-235 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20220707 N/A ANDA ANDA205101 Asclemed USA, Inc. GABAPENTIN 600 mg/1 120 TABLET in 1 BOTTLE (76420-235-12)
76420-235-24 76420-235 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20220707 N/A ANDA ANDA205101 Asclemed USA, Inc. GABAPENTIN 600 mg/1 240 TABLET in 1 BOTTLE (76420-235-24)
76420-235-60 76420-235 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20220707 N/A ANDA ANDA205101 Asclemed USA, Inc. GABAPENTIN 600 mg/1 60 TABLET in 1 BOTTLE (76420-235-60)
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)
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