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
16714-758-01 16714-758 HUMAN PRESCRIPTION DRUG atomoxetine atomoxetine CAPSULE ORAL 20180601 N/A ANDA ANDA079019 Northstar Rx LLC ATOMOXETINE HYDROCHLORIDE 40 mg/1 30 CAPSULE in 1 BOTTLE (16714-758-01)
50090-7342-0 50090-7342 HUMAN PRESCRIPTION DRUG atomoxetine atomoxetine CAPSULE ORAL 20241016 N/A ANDA ANDA079019 A-S Medication Solutions ATOMOXETINE HYDROCHLORIDE 25 mg/1 30 CAPSULE in 1 BOTTLE (50090-7342-0)
50090-7397-0 50090-7397 HUMAN PRESCRIPTION DRUG atomoxetine atomoxetine CAPSULE ORAL 20241023 N/A ANDA ANDA079019 A-S Medication Solutions ATOMOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE in 1 BOTTLE (50090-7397-0)
50090-7462-0 50090-7462 HUMAN PRESCRIPTION DRUG atomoxetine atomoxetine CAPSULE ORAL 20241119 N/A ANDA ANDA079019 A-S Medication Solutions ATOMOXETINE HYDROCHLORIDE 40 mg/1 30 CAPSULE in 1 BOTTLE (50090-7462-0)
50090-7463-0 50090-7463 HUMAN PRESCRIPTION DRUG atomoxetine atomoxetine CAPSULE ORAL 20241119 N/A ANDA ANDA079019 A-S Medication Solutions ATOMOXETINE HYDROCHLORIDE 100 mg/1 30 CAPSULE in 1 BOTTLE (50090-7463-0)
71335-2361-1 71335-2361 HUMAN PRESCRIPTION DRUG atomoxetine atomoxetine CAPSULE ORAL 20240528 N/A ANDA ANDA079019 Bryant Ranch Prepack ATOMOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE in 1 BOTTLE (71335-2361-1)
71335-2361-2 71335-2361 HUMAN PRESCRIPTION DRUG atomoxetine atomoxetine CAPSULE ORAL 20240528 N/A ANDA ANDA079019 Bryant Ranch Prepack ATOMOXETINE HYDROCHLORIDE 60 mg/1 60 CAPSULE in 1 BOTTLE (71335-2361-2)
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