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 66 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
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)
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)
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)
70518-3815-6 70518-3815 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20260513 N/A NDA AUTHORIZED GENERIC NDA010721 REMEDYREPACK INC. MECLIZINE HYDROCHLORIDE 25 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (70518-3815-6)
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)
16571-662-01 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)
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)
72189-302-30 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)
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)
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)
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