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"
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
70199-002-01 70199-002 HUMAN PRESCRIPTION DRUG Antivert meclizine HCl TABLET ORAL 20200115 N/A NDA NDA010721 Casper Pharma LLC MECLIZINE HYDROCHLORIDE 12.5 mg/1 100 TABLET in 1 BOTTLE (70199-002-01)
70199-002-05 70199-002 HUMAN PRESCRIPTION DRUG Antivert meclizine HCl TABLET ORAL 20200115 N/A NDA NDA010721 Casper Pharma LLC MECLIZINE HYDROCHLORIDE 12.5 mg/1 500 TABLET in 1 BOTTLE (70199-002-05)
70199-003-01 70199-003 HUMAN PRESCRIPTION DRUG Antivert meclizine HCl TABLET ORAL 20200115 N/A NDA NDA010721 Casper Pharma LLC MECLIZINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (70199-003-01)
70199-003-99 70199-003 HUMAN PRESCRIPTION DRUG Antivert meclizine HCl TABLET ORAL 20200115 N/A NDA NDA010721 Casper Pharma LLC MECLIZINE HYDROCHLORIDE 25 mg/1 1000 TABLET in 1 BOTTLE (70199-003-99)
70199-004-01 70199-004 HUMAN PRESCRIPTION DRUG Antivert meclizine hcl TABLET ORAL 20200115 N/A NDA NDA010721 Casper Pharma LLC MECLIZINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (70199-004-01)
70199-004-99 70199-004 HUMAN PRESCRIPTION DRUG Antivert meclizine hcl TABLET ORAL 20200115 N/A NDA NDA010721 Casper Pharma LLC MECLIZINE HYDROCHLORIDE 50 mg/1 1000 TABLET in 1 BOTTLE (70199-004-99)
70199-018-01 70199-018 HUMAN PRESCRIPTION DRUG Antivert meclizine hcl TABLET, CHEWABLE ORAL 20200115 N/A NDA NDA010721 Casper Pharma LLC MECLIZINE HYDROCHLORIDE 25 mg/1 100 TABLET, CHEWABLE in 1 BOTTLE (70199-018-01)
71205-647-10 71205-647 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20220323 N/A NDA AUTHORIZED GENERIC NDA010721 Proficient Rx LP MECLIZINE HYDROCHLORIDE 12.5 mg/1 10 TABLET in 1 BOTTLE (71205-647-10)
71205-647-90 71205-647 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20220323 N/A NDA AUTHORIZED GENERIC NDA010721 Proficient Rx LP MECLIZINE HYDROCHLORIDE 12.5 mg/1 90 TABLET in 1 BOTTLE (71205-647-90)
71335-1825-0 71335-1825 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20220224 N/A NDA AUTHORIZED GENERIC NDA010721 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 14 TABLET in 1 BOTTLE (71335-1825-0)
71335-1825-1 71335-1825 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20220224 N/A NDA AUTHORIZED GENERIC NDA010721 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 90 TABLET in 1 BOTTLE (71335-1825-1)
71335-1825-2 71335-1825 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20220224 N/A NDA AUTHORIZED GENERIC NDA010721 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE (71335-1825-2)
71335-1825-3 71335-1825 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20220224 N/A NDA AUTHORIZED GENERIC NDA010721 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 25 TABLET in 1 BOTTLE (71335-1825-3)
71335-1825-4 71335-1825 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20220224 N/A NDA AUTHORIZED GENERIC NDA010721 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 20 TABLET in 1 BOTTLE (71335-1825-4)
71335-1825-5 71335-1825 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20220224 N/A NDA AUTHORIZED GENERIC NDA010721 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 40 TABLET in 1 BOTTLE (71335-1825-5)
71335-1825-6 71335-1825 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20220224 N/A NDA AUTHORIZED GENERIC NDA010721 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 60 TABLET in 1 BOTTLE (71335-1825-6)
71335-1825-7 71335-1825 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20220224 N/A NDA AUTHORIZED GENERIC NDA010721 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 120 TABLET in 1 BOTTLE (71335-1825-7)
71335-1825-8 71335-1825 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20220224 N/A NDA AUTHORIZED GENERIC NDA010721 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 10 TABLET in 1 BOTTLE (71335-1825-8)
71335-1825-9 71335-1825 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20220224 N/A NDA AUTHORIZED GENERIC NDA010721 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (71335-1825-9)
71335-1872-1 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 30 TABLET in 1 BOTTLE (71335-1872-1)
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