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=ANDA217116"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
70010-227-01 70010-227 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20230627 N/A ANDA ANDA217116 Granules Pharmaceuticals Inc. GABAPENTIN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70010-227-01)
70010-227-05 70010-227 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20230627 N/A ANDA ANDA217116 Granules Pharmaceuticals Inc. GABAPENTIN 600 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (70010-227-05)
70010-228-01 70010-228 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20230627 N/A ANDA ANDA217116 Granules Pharmaceuticals Inc. GABAPENTIN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70010-228-01)
70010-228-05 70010-228 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20230627 N/A ANDA ANDA217116 Granules Pharmaceuticals Inc. GABAPENTIN 800 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (70010-228-05)
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