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=ANDA203934"
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
70771-1917-1 70771-1917 HUMAN PRESCRIPTION DRUG gabapentin gabapentin TABLET ORAL 20250918 N/A ANDA ANDA203934 Zydus Lifesciences Limited GABAPENTIN 750 mg/1 100 TABLET in 1 BOTTLE (70771-1917-1)
70771-1917-6 70771-1917 HUMAN PRESCRIPTION DRUG gabapentin gabapentin TABLET ORAL 20250918 N/A ANDA ANDA203934 Zydus Lifesciences Limited GABAPENTIN 750 mg/1 60 TABLET in 1 BOTTLE (70771-1917-6)
68382-355-14 68382-355 HUMAN PRESCRIPTION DRUG gabapentin gabapentin TABLET ORAL 20250918 N/A ANDA ANDA203934 Zydus Pharmaceuticals USA Inc. GABAPENTIN 450 mg/1 60 TABLET in 1 BOTTLE (68382-355-14)
68382-355-01 68382-355 HUMAN PRESCRIPTION DRUG gabapentin gabapentin TABLET ORAL 20250918 N/A ANDA ANDA203934 Zydus Pharmaceuticals USA Inc. GABAPENTIN 450 mg/1 100 TABLET in 1 BOTTLE (68382-355-01)
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