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=ANDA200651"
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
82009-071-05 82009-071 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20230901 N/A ANDA ANDA200651 QUALLENT PHARMACEUTICALS HEALTH LLC GABAPENTIN 600 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (82009-071-05)
82009-072-05 82009-072 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20230901 N/A ANDA ANDA200651 QUALLENT PHARMACEUTICALS HEALTH LLC GABAPENTIN 800 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (82009-072-05)
63187-148-90 63187-148 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA200651 Proficient Rx LP GABAPENTIN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-148-90)
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