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=NDA010721"
符合检索条件的记录共 66 条，共 4 页，当前第 2 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
71335-1872-2 71335-1872 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20210628 N/A NDA AUTHORIZED GENERIC NDA010721 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 12.5 mg/1 60 TABLET in 1 BOTTLE (71335-1872-2)
71335-1872-3 71335-1872 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20210628 N/A NDA AUTHORIZED GENERIC NDA010721 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 12.5 mg/1 90 TABLET in 1 BOTTLE (71335-1872-3)
71335-1872-4 71335-1872 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20210628 N/A NDA AUTHORIZED GENERIC NDA010721 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 12.5 mg/1 28 TABLET in 1 BOTTLE (71335-1872-4)
71335-1872-5 71335-1872 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20210628 N/A NDA AUTHORIZED GENERIC NDA010721 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 12.5 mg/1 20 TABLET in 1 BOTTLE (71335-1872-5)
71335-1872-6 71335-1872 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20210628 N/A NDA AUTHORIZED GENERIC NDA010721 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 12.5 mg/1 120 TABLET in 1 BOTTLE (71335-1872-6)
71335-1872-7 71335-1872 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20210628 N/A NDA AUTHORIZED GENERIC NDA010721 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 12.5 mg/1 100 TABLET in 1 BOTTLE (71335-1872-7)
71335-1872-8 71335-1872 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20210628 N/A NDA AUTHORIZED GENERIC NDA010721 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 12.5 mg/1 10 TABLET in 1 BOTTLE (71335-1872-8)
76420-799-01 76420-799 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20240405 N/A NDA AUTHORIZED GENERIC NDA010721 Asclemed USA, Inc. MECLIZINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (76420-799-01)
76420-799-30 76420-799 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20240405 N/A NDA AUTHORIZED GENERIC NDA010721 Asclemed USA, Inc. MECLIZINE HYDROCHLORIDE 50 mg/1 30 TABLET in 1 BOTTLE (76420-799-30)
76420-799-60 76420-799 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20240405 N/A NDA AUTHORIZED GENERIC NDA010721 Asclemed USA, Inc. MECLIZINE HYDROCHLORIDE 50 mg/1 60 TABLET in 1 BOTTLE (76420-799-60)
76420-799-90 76420-799 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20240405 N/A NDA AUTHORIZED GENERIC NDA010721 Asclemed USA, Inc. MECLIZINE HYDROCHLORIDE 50 mg/1 90 TABLET in 1 BOTTLE (76420-799-90)
71205-786-10 71205-786 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20230403 N/A NDA AUTHORIZED GENERIC NDA010721 Proficient Rx LP MECLIZINE HYDROCHLORIDE 25 mg/1 10 TABLET in 1 BOTTLE (71205-786-10)
71205-786-20 71205-786 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20230403 N/A NDA AUTHORIZED GENERIC NDA010721 Proficient Rx LP MECLIZINE HYDROCHLORIDE 25 mg/1 20 TABLET in 1 BOTTLE (71205-786-20)
71205-786-30 71205-786 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20230403 N/A NDA AUTHORIZED GENERIC NDA010721 Proficient Rx LP MECLIZINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE (71205-786-30)
71205-786-60 71205-786 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20230403 N/A NDA AUTHORIZED GENERIC NDA010721 Proficient Rx LP MECLIZINE HYDROCHLORIDE 25 mg/1 60 TABLET in 1 BOTTLE (71205-786-60)
71205-786-90 71205-786 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20230403 N/A NDA AUTHORIZED GENERIC NDA010721 Proficient Rx LP MECLIZINE HYDROCHLORIDE 25 mg/1 90 TABLET in 1 BOTTLE (71205-786-90)
16571-660-01 16571-660 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20200115 N/A NDA AUTHORIZED GENERIC NDA010721 Rising Pharma Holdings, Inc. MECLIZINE HYDROCHLORIDE 12.5 mg/1 100 TABLET in 1 BOTTLE (16571-660-01)
76420-798-01 76420-798 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20240405 N/A NDA AUTHORIZED GENERIC NDA010721 Asclemed USA, Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (76420-798-01)
76420-798-30 76420-798 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20240405 N/A NDA AUTHORIZED GENERIC NDA010721 Asclemed USA, Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE (76420-798-30)
76420-798-60 76420-798 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20240405 N/A NDA AUTHORIZED GENERIC NDA010721 Asclemed USA, Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 60 TABLET in 1 BOTTLE (76420-798-60)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase