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 64 条，共 4 页，当前第 2 页 ，可点击列名称排序
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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
71335-1825-7 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)
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)
70518-3768-0 70518-3768 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20230619 N/A NDA AUTHORIZED GENERIC NDA010721 REMEDYREPACK INC. MECLIZINE HYDROCHLORIDE 12.5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (70518-3768-0)
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)
70518-3815-1 70518-3815 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20240406 N/A NDA AUTHORIZED GENERIC NDA010721 REMEDYREPACK INC. MECLIZINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (70518-3815-1)
70518-3815-2 70518-3815 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20250207 N/A NDA AUTHORIZED GENERIC NDA010721 REMEDYREPACK INC. MECLIZINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BLISTER PACK (70518-3815-2)
70518-3815-3 70518-3815 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20250913 N/A NDA AUTHORIZED GENERIC NDA010721 REMEDYREPACK INC. MECLIZINE HYDROCHLORIDE 25 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (70518-3815-3)
70518-3815-4 70518-3815 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20260112 N/A NDA AUTHORIZED GENERIC NDA010721 REMEDYREPACK INC. MECLIZINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (70518-3815-4)
70518-3815-5 70518-3815 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20260217 N/A NDA AUTHORIZED GENERIC NDA010721 REMEDYREPACK INC. MECLIZINE HYDROCHLORIDE 25 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (70518-3815-5)
68071-2380-2 68071-2380 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20210329 N/A NDA AUTHORIZED GENERIC NDA010721 NuCare Pharmaceuticals,Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 20 TABLET in 1 BOTTLE (68071-2380-2)
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