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"
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
76420-797-60 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)
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)
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)
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)
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)
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)
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