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 61 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
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)
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)
71205-786-60 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)
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)
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)
76420-797-60 76420-797 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20240405 N/A NDA AUTHORIZED GENERIC NDA010721 Asclemed USA, Inc. MECLIZINE HYDROCHLORIDE 12.5 mg/1 60 TABLET in 1 BOTTLE (76420-797-60)
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)
76420-798-90 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 90 TABLET in 1 BOTTLE (76420-798-90)
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)
76420-797-90 76420-797 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20240405 N/A NDA AUTHORIZED GENERIC NDA010721 Asclemed USA, Inc. MECLIZINE HYDROCHLORIDE 12.5 mg/1 90 TABLET in 1 BOTTLE (76420-797-90)
76420-797-01 76420-797 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20240405 N/A NDA AUTHORIZED GENERIC NDA010721 Asclemed USA, Inc. MECLIZINE HYDROCHLORIDE 12.5 mg/1 100 TABLET in 1 BOTTLE (76420-797-01)
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