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=ANDA076001"
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
71335-0924-3 71335-0924 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine CAPSULE ORAL 20190405 N/A ANDA ANDA076001 Bryant Ranch Prepack FLUOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE in 1 BOTTLE (71335-0924-3)
71335-0924-4 71335-0924 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine CAPSULE ORAL 20220921 N/A ANDA ANDA076001 Bryant Ranch Prepack FLUOXETINE HYDROCHLORIDE 20 mg/1 15 CAPSULE in 1 BOTTLE (71335-0924-4)
71335-0924-5 71335-0924 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine CAPSULE ORAL 20220921 N/A ANDA ANDA076001 Bryant Ranch Prepack FLUOXETINE HYDROCHLORIDE 20 mg/1 56 CAPSULE in 1 BOTTLE (71335-0924-5)
71335-0924-6 71335-0924 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine CAPSULE ORAL 20220921 N/A ANDA ANDA076001 Bryant Ranch Prepack FLUOXETINE HYDROCHLORIDE 20 mg/1 28 CAPSULE in 1 BOTTLE (71335-0924-6)
71335-0924-7 71335-0924 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine CAPSULE ORAL 20180905 N/A ANDA ANDA076001 Bryant Ranch Prepack FLUOXETINE HYDROCHLORIDE 20 mg/1 90 CAPSULE in 1 BOTTLE (71335-0924-7)
71335-0924-8 71335-0924 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine CAPSULE ORAL 20220921 N/A ANDA ANDA076001 Bryant Ranch Prepack FLUOXETINE HYDROCHLORIDE 20 mg/1 120 CAPSULE in 1 BOTTLE (71335-0924-8)
71335-0924-9 71335-0924 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine CAPSULE ORAL 20220921 N/A ANDA ANDA076001 Bryant Ranch Prepack FLUOXETINE HYDROCHLORIDE 20 mg/1 45 CAPSULE in 1 BOTTLE (71335-0924-9)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase