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=ANDA075452"
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
71205-188-30 71205-188 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine CAPSULE ORAL 20190101 N/A ANDA ANDA075452 Proficient Rx LP FLUOXETINE HYDROCHLORIDE 40 mg/1 30 CAPSULE in 1 BOTTLE (71205-188-30)
71205-188-60 71205-188 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine CAPSULE ORAL 20190101 N/A ANDA ANDA075452 Proficient Rx LP FLUOXETINE HYDROCHLORIDE 40 mg/1 60 CAPSULE in 1 BOTTLE (71205-188-60)
71205-188-90 71205-188 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine CAPSULE ORAL 20190101 N/A ANDA ANDA075452 Proficient Rx LP FLUOXETINE HYDROCHLORIDE 40 mg/1 90 CAPSULE in 1 BOTTLE (71205-188-90)
42291-398-01 42291-398 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine CAPSULE ORAL 20170814 N/A ANDA ANDA075452 AvKARE FLUOXETINE HYDROCHLORIDE 40 mg/1 100 CAPSULE in 1 BOTTLE (42291-398-01)
42291-398-50 42291-398 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine CAPSULE ORAL 20170814 N/A ANDA ANDA075452 AvKARE FLUOXETINE HYDROCHLORIDE 40 mg/1 500 CAPSULE in 1 BOTTLE (42291-398-50)
0093-7198-01 0093-7198 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine CAPSULE ORAL 20080908 N/A ANDA ANDA075452 Teva Pharmaceuticals USA, Inc. FLUOXETINE HYDROCHLORIDE 40 mg/1 100 CAPSULE in 1 BOTTLE (0093-7198-01)
0093-7198-05 0093-7198 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine CAPSULE ORAL 20080923 N/A ANDA ANDA075452 Teva Pharmaceuticals USA, Inc. FLUOXETINE HYDROCHLORIDE 40 mg/1 500 CAPSULE in 1 BOTTLE (0093-7198-05)
0093-7198-56 0093-7198 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine CAPSULE ORAL 20020130 N/A ANDA ANDA075452 Teva Pharmaceuticals USA, Inc. FLUOXETINE HYDROCHLORIDE 40 mg/1 30 CAPSULE in 1 BOTTLE (0093-7198-56)
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