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=ANDA204989"
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
68788-8816-1 68788-8816 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20250121 N/A ANDA ANDA204989 Preferred Pharmaceuticals Inc. GABAPENTIN 400 mg/1 100 CAPSULE in 1 BOTTLE, PLASTIC (68788-8816-1)
68788-8816-9 68788-8816 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20250121 N/A ANDA ANDA204989 Preferred Pharmaceuticals Inc. GABAPENTIN 400 mg/1 90 CAPSULE in 1 BOTTLE, PLASTIC (68788-8816-9)
68788-8816-3 68788-8816 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20250121 N/A ANDA ANDA204989 Preferred Pharmaceuticals Inc. GABAPENTIN 400 mg/1 30 CAPSULE in 1 BOTTLE, PLASTIC (68788-8816-3)
68788-8816-6 68788-8816 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20250121 N/A ANDA ANDA204989 Preferred Pharmaceuticals Inc. GABAPENTIN 400 mg/1 60 CAPSULE in 1 BOTTLE, PLASTIC (68788-8816-6)
68788-8816-8 68788-8816 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20250121 N/A ANDA ANDA204989 Preferred Pharmaceuticals Inc. GABAPENTIN 400 mg/1 120 CAPSULE in 1 BOTTLE, PLASTIC (68788-8816-8)
69367-131-06 69367-131 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20160401 20261201 ANDA ANDA204989 Westminster Pharmaceuticals, LLC GABAPENTIN 100 mg/1 500 CAPSULE in 1 BOTTLE (69367-131-06)
69367-132-06 69367-132 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20160401 20261201 ANDA ANDA204989 Westminster Pharmaceuticals, LLC GABAPENTIN 300 mg/1 500 CAPSULE in 1 BOTTLE (69367-132-06)
69367-133-06 69367-133 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20160401 20261201 ANDA ANDA204989 Westminster Pharmaceuticals, LLC GABAPENTIN 400 mg/1 500 CAPSULE in 1 BOTTLE (69367-133-06)
71205-766-30 71205-766 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20230221 N/A ANDA ANDA204989 Proficient Rx LP GABAPENTIN 300 mg/1 30 CAPSULE in 1 BOTTLE, PLASTIC (71205-766-30)
71205-766-60 71205-766 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20230221 N/A ANDA ANDA204989 Proficient Rx LP GABAPENTIN 300 mg/1 60 CAPSULE in 1 BOTTLE, PLASTIC (71205-766-60)
71205-766-90 71205-766 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20230221 N/A ANDA ANDA204989 Proficient Rx LP GABAPENTIN 300 mg/1 90 CAPSULE in 1 BOTTLE, PLASTIC (71205-766-90)
71205-766-14 71205-766 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20240320 N/A ANDA ANDA204989 Proficient Rx LP GABAPENTIN 300 mg/1 14 CAPSULE in 1 BOTTLE, PLASTIC (71205-766-14)
71205-808-30 71205-808 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20230525 N/A ANDA ANDA204989 Proficient Rx LP GABAPENTIN 400 mg/1 30 CAPSULE in 1 BOTTLE (71205-808-30)
71205-808-60 71205-808 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20230525 N/A ANDA ANDA204989 Proficient Rx LP GABAPENTIN 400 mg/1 60 CAPSULE in 1 BOTTLE (71205-808-60)
71205-808-90 71205-808 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20230525 N/A ANDA ANDA204989 Proficient Rx LP GABAPENTIN 400 mg/1 90 CAPSULE in 1 BOTTLE (71205-808-90)
71205-928-30 71205-928 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20210422 N/A ANDA ANDA204989 Proficient Rx LP GABAPENTIN 100 mg/1 30 CAPSULE in 1 BOTTLE (71205-928-30)
71205-928-64 71205-928 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20210422 N/A ANDA ANDA204989 Proficient Rx LP GABAPENTIN 100 mg/1 240 CAPSULE in 1 BOTTLE (71205-928-64)
71205-928-55 71205-928 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20210422 N/A ANDA ANDA204989 Proficient Rx LP GABAPENTIN 100 mg/1 500 CAPSULE in 1 BOTTLE (71205-928-55)
71205-928-60 71205-928 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20210422 N/A ANDA ANDA204989 Proficient Rx LP GABAPENTIN 100 mg/1 60 CAPSULE in 1 BOTTLE (71205-928-60)
71205-928-00 71205-928 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin CAPSULE ORAL 20210422 N/A ANDA ANDA204989 Proficient Rx LP GABAPENTIN 100 mg/1 100 CAPSULE in 1 BOTTLE (71205-928-00)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase