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 3 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
80425-0494-1 80425-0494 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20250202 N/A NDA AUTHORIZED GENERIC NDA010721 Advanced Rx of Tennessee, LLC MECLIZINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE (80425-0494-1)
80425-0494-2 80425-0494 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20250202 N/A NDA AUTHORIZED GENERIC NDA010721 Advanced Rx of Tennessee, LLC MECLIZINE HYDROCHLORIDE 25 mg/1 60 TABLET in 1 BOTTLE (80425-0494-2)
80425-0494-3 80425-0494 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20250202 N/A NDA AUTHORIZED GENERIC NDA010721 Advanced Rx of Tennessee, LLC MECLIZINE HYDROCHLORIDE 25 mg/1 90 TABLET in 1 BOTTLE (80425-0494-3)
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)
68071-2380-3 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 30 TABLET in 1 BOTTLE (68071-2380-3)
68071-2380-9 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 90 TABLET in 1 BOTTLE (68071-2380-9)
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)
68788-8633-1 68788-8633 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20240416 N/A NDA AUTHORIZED GENERIC NDA010721 Preferred Pharmaceuticals Inc. MECLIZINE HYDROCHLORIDE 12.5 mg/1 10 TABLET in 1 BOTTLE (68788-8633-1)
68788-8633-3 68788-8633 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20240416 N/A NDA AUTHORIZED GENERIC NDA010721 Preferred Pharmaceuticals Inc. MECLIZINE HYDROCHLORIDE 12.5 mg/1 30 TABLET in 1 BOTTLE (68788-8633-3)
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)
68071-2416-6 68071-2416 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20210524 N/A NDA AUTHORIZED GENERIC NDA010721 NuCare Pharmaceuticals,Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 6 TABLET in 1 BOTTLE (68071-2416-6)
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)
16571-660-50 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/1 500 TABLET in 1 BOTTLE (16571-660-50)
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)
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)
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