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 62 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
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)
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)
72189-302-30 72189-302 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE MECLIZINE HYDROCHLORIDE TABLET ORAL 20211206 N/A NDA AUTHORIZED GENERIC NDA010721 DirectRx MECLIZINE HYDROCHLORIDE 12.5 mg/1 30 TABLET in 1 BOTTLE (72189-302-30)
72189-302-60 72189-302 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE MECLIZINE HYDROCHLORIDE TABLET ORAL 20211206 N/A NDA AUTHORIZED GENERIC NDA010721 DirectRx MECLIZINE HYDROCHLORIDE 12.5 mg/1 60 TABLET in 1 BOTTLE (72189-302-60)
16571-660-01 16571-660 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20200115 N/A NDA AUTHORIZED GENERIC NDA010721 Rising Pharmaceuticals, 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 Pharmaceuticals, Inc. MECLIZINE HYDROCHLORIDE 12.5 mg/1 500 TABLET in 1 BOTTLE (16571-660-50)
16571-661-01 16571-661 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20200115 N/A NDA AUTHORIZED GENERIC NDA010721 Rising Pharmaceuticals, Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (16571-661-01)
16571-661-10 16571-661 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20200115 N/A NDA AUTHORIZED GENERIC NDA010721 Rising Pharmaceuticals, Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 1000 TABLET in 1 BOTTLE (16571-661-10)
16571-662-01 16571-662 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20200115 N/A NDA AUTHORIZED GENERIC NDA010721 Rising Pharmaceuticals, Inc. MECLIZINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (16571-662-01)
16571-663-01 16571-663 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET, CHEWABLE ORAL 20200115 N/A NDA AUTHORIZED GENERIC NDA010721 Rising Pharmaceuticals, Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 100 TABLET, CHEWABLE in 1 BOTTLE (16571-663-01)
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)
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