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 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
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)
72189-237-30 72189-237 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20220901 N/A NDA AUTHORIZED GENERIC NDA010721 Direct_Rx MECLIZINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE (72189-237-30)
72189-237-90 72189-237 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20220901 N/A NDA AUTHORIZED GENERIC NDA010721 Direct_Rx MECLIZINE HYDROCHLORIDE 25 mg/1 90 TABLET in 1 BOTTLE (72189-237-90)
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)
76420-797-30 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 30 TABLET in 1 BOTTLE (76420-797-30)
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)
76420-797-90 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)
60760-661-30 60760-661 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20210621 N/A NDA AUTHORIZED GENERIC NDA010721 St. Mary's Medical Park Pharmacy MECLIZINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (60760-661-30)
60760-661-90 60760-661 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20220201 N/A NDA AUTHORIZED GENERIC NDA010721 St. Mary's Medical Park Pharmacy MECLIZINE HYDROCHLORIDE 25 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (60760-661-90)
16571-663-01 16571-663 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET, CHEWABLE ORAL 20200115 N/A NDA AUTHORIZED GENERIC NDA010721 Rising Pharma Holdings, Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 100 TABLET, CHEWABLE in 1 BOTTLE (16571-663-01)
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)
67296-1432-3 67296-1432 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20210301 N/A NDA AUTHORIZED GENERIC NDA010721 RedPharm Drug, Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE (67296-1432-3)
67296-1432-7 67296-1432 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20200115 N/A NDA AUTHORIZED GENERIC NDA010721 RedPharm Drug, Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 21 TABLET in 1 BOTTLE (67296-1432-7)
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)
16571-662-01 16571-662 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20200115 N/A NDA AUTHORIZED GENERIC NDA010721 Rising Pharma Holdings, Inc. MECLIZINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (16571-662-01)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase