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=ANDA203244"
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
71205-160-30 71205-160 HUMAN PRESCRIPTION DRUG Gabapentin GABAPENTIN TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA203244 Proficient Rx LP GABAPENTIN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-160-30)
71205-160-60 71205-160 HUMAN PRESCRIPTION DRUG Gabapentin GABAPENTIN TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA203244 Proficient Rx LP GABAPENTIN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-160-60)
71205-160-90 71205-160 HUMAN PRESCRIPTION DRUG Gabapentin GABAPENTIN TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA203244 Proficient Rx LP GABAPENTIN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-160-90)
71205-457-30 71205-457 HUMAN PRESCRIPTION DRUG Gabapentin GABAPENTIN TABLET, FILM COATED ORAL 20200623 N/A ANDA ANDA203244 Proficient Rx LP GABAPENTIN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-457-30)
71205-457-60 71205-457 HUMAN PRESCRIPTION DRUG Gabapentin GABAPENTIN TABLET, FILM COATED ORAL 20200623 N/A ANDA ANDA203244 Proficient Rx LP GABAPENTIN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-457-60)
71205-457-90 71205-457 HUMAN PRESCRIPTION DRUG Gabapentin GABAPENTIN TABLET, FILM COATED ORAL 20200623 N/A ANDA ANDA203244 Proficient Rx LP GABAPENTIN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-457-90)
64380-727-01 64380-727 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20251110 N/A ANDA ANDA203244 Strides Pharma Science Limited GABAPENTIN 600 mg/1 100 TABLET in 1 CONTAINER (64380-727-01)
64380-727-02 64380-727 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20251110 N/A ANDA ANDA203244 Strides Pharma Science Limited GABAPENTIN 600 mg/1 500 TABLET in 1 CONTAINER (64380-727-02)
64380-728-01 64380-728 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20251110 N/A ANDA ANDA203244 Strides Pharma Science Limited GABAPENTIN 800 mg/1 100 TABLET in 1 CONTAINER (64380-728-01)
64380-728-02 64380-728 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20251110 N/A ANDA ANDA203244 Strides Pharma Science Limited GABAPENTIN 800 mg/1 500 TABLET in 1 CONTAINER (64380-728-02)
72162-2141-1 72162-2141 HUMAN PRESCRIPTION DRUG Gabapentin GABAPENTIN TABLET, FILM COATED ORAL 20231012 N/A ANDA ANDA203244 Bryant Ranch Prepack GABAPENTIN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72162-2141-1)
72162-2141-5 72162-2141 HUMAN PRESCRIPTION DRUG Gabapentin GABAPENTIN TABLET, FILM COATED ORAL 20231012 N/A ANDA ANDA203244 Bryant Ranch Prepack GABAPENTIN 600 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72162-2141-5)
72162-2142-1 72162-2142 HUMAN PRESCRIPTION DRUG Gabapentin GABAPENTIN TABLET, FILM COATED ORAL 20231012 N/A ANDA ANDA203244 Bryant Ranch Prepack GABAPENTIN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72162-2142-1)
72162-2142-5 72162-2142 HUMAN PRESCRIPTION DRUG Gabapentin GABAPENTIN TABLET, FILM COATED ORAL 20231012 N/A ANDA ANDA203244 Bryant Ranch Prepack GABAPENTIN 800 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72162-2142-5)
70518-2098-0 70518-2098 HUMAN PRESCRIPTION DRUG Gabapentin GABAPENTIN TABLET, FILM COATED ORAL 20190522 N/A ANDA ANDA203244 REMEDYREPACK INC. GABAPENTIN 600 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2098-0)
68788-8687-6 68788-8687 HUMAN PRESCRIPTION DRUG Gabapentin GABAPENTIN TABLET, FILM COATED ORAL 20240605 N/A ANDA ANDA203244 Preferred Pharmaceuticals Inc. GABAPENTIN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8687-6)
68788-8687-3 68788-8687 HUMAN PRESCRIPTION DRUG Gabapentin GABAPENTIN TABLET, FILM COATED ORAL 20240605 N/A ANDA ANDA203244 Preferred Pharmaceuticals Inc. GABAPENTIN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8687-3)
68788-8688-1 68788-8688 HUMAN PRESCRIPTION DRUG Gabapentin GABAPENTIN TABLET, FILM COATED ORAL 20240605 N/A ANDA ANDA203244 Preferred Pharmaceuticals Inc. GABAPENTIN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-8688-1)
68788-8688-3 68788-8688 HUMAN PRESCRIPTION DRUG Gabapentin GABAPENTIN TABLET, FILM COATED ORAL 20240605 N/A ANDA ANDA203244 Preferred Pharmaceuticals Inc. GABAPENTIN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8688-3)
68788-8688-6 68788-8688 HUMAN PRESCRIPTION DRUG Gabapentin GABAPENTIN TABLET, FILM COATED ORAL 20240605 N/A ANDA ANDA203244 Preferred Pharmaceuticals Inc. GABAPENTIN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8688-6)
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