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=ANDA079019"
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
68462-268-30 68462-268 HUMAN PRESCRIPTION DRUG atomoxetine atomoxetine CAPSULE ORAL 20170530 N/A ANDA ANDA079019 Glenmark Pharmaceuticals Inc., USA ATOMOXETINE HYDROCHLORIDE 40 mg/1 30 CAPSULE in 1 BOTTLE (68462-268-30)
68462-269-23 68462-269 HUMAN PRESCRIPTION DRUG atomoxetine atomoxetine CAPSULE ORAL 20170530 N/A ANDA ANDA079019 Glenmark Pharmaceuticals Inc., USA ATOMOXETINE HYDROCHLORIDE 60 mg/1 2000 CAPSULE in 1 BOTTLE (68462-269-23)
68462-269-30 68462-269 HUMAN PRESCRIPTION DRUG atomoxetine atomoxetine CAPSULE ORAL 20170530 N/A ANDA ANDA079019 Glenmark Pharmaceuticals Inc., USA ATOMOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE in 1 BOTTLE (68462-269-30)
68462-270-23 68462-270 HUMAN PRESCRIPTION DRUG atomoxetine atomoxetine CAPSULE ORAL 20170530 N/A ANDA ANDA079019 Glenmark Pharmaceuticals Inc., USA ATOMOXETINE HYDROCHLORIDE 80 mg/1 2000 CAPSULE in 1 BOTTLE (68462-270-23)
68462-270-30 68462-270 HUMAN PRESCRIPTION DRUG atomoxetine atomoxetine CAPSULE ORAL 20170530 N/A ANDA ANDA079019 Glenmark Pharmaceuticals Inc., USA ATOMOXETINE HYDROCHLORIDE 80 mg/1 30 CAPSULE in 1 BOTTLE (68462-270-30)
68462-271-30 68462-271 HUMAN PRESCRIPTION DRUG atomoxetine atomoxetine CAPSULE ORAL 20170530 N/A ANDA ANDA079019 Glenmark Pharmaceuticals Inc., USA ATOMOXETINE HYDROCHLORIDE 100 mg/1 30 CAPSULE in 1 BOTTLE (68462-271-30)
68462-271-51 68462-271 HUMAN PRESCRIPTION DRUG atomoxetine atomoxetine CAPSULE ORAL 20170530 N/A ANDA ANDA079019 Glenmark Pharmaceuticals Inc., USA ATOMOXETINE HYDROCHLORIDE 100 mg/1 1500 CAPSULE in 1 BOTTLE (68462-271-51)
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