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=ANDA078021"
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
65862-103-05 65862-103 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20070717 N/A ANDA ANDA078021 Aurobindo Pharma Limited AMLODIPINE BESYLATE 10 mg/1 500 TABLET in 1 BOTTLE (65862-103-05)
65862-103-30 65862-103 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20070717 N/A ANDA ANDA078021 Aurobindo Pharma Limited AMLODIPINE BESYLATE 10 mg/1 30 TABLET in 1 BOTTLE (65862-103-30)
65862-103-90 65862-103 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20070717 N/A ANDA ANDA078021 Aurobindo Pharma Limited AMLODIPINE BESYLATE 10 mg/1 90 TABLET in 1 BOTTLE (65862-103-90)
65862-103-99 65862-103 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20070717 N/A ANDA ANDA078021 Aurobindo Pharma Limited AMLODIPINE BESYLATE 10 mg/1 1000 TABLET in 1 BOTTLE (65862-103-99)
65862-101-05 65862-101 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20070717 N/A ANDA ANDA078021 Aurobindo Pharma Limited AMLODIPINE BESYLATE 2.5 mg/1 500 TABLET in 1 BOTTLE (65862-101-05)
65862-101-30 65862-101 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20070717 N/A ANDA ANDA078021 Aurobindo Pharma Limited AMLODIPINE BESYLATE 2.5 mg/1 30 TABLET in 1 BOTTLE (65862-101-30)
65862-101-90 65862-101 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20070717 N/A ANDA ANDA078021 Aurobindo Pharma Limited AMLODIPINE BESYLATE 2.5 mg/1 90 TABLET in 1 BOTTLE (65862-101-90)
65862-101-99 65862-101 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20070717 N/A ANDA ANDA078021 Aurobindo Pharma Limited AMLODIPINE BESYLATE 2.5 mg/1 1000 TABLET in 1 BOTTLE (65862-101-99)
65862-102-05 65862-102 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20070717 N/A ANDA ANDA078021 Aurobindo Pharma Limited AMLODIPINE BESYLATE 5 mg/1 500 TABLET in 1 BOTTLE (65862-102-05)
65862-102-30 65862-102 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20070717 N/A ANDA ANDA078021 Aurobindo Pharma Limited AMLODIPINE BESYLATE 5 mg/1 30 TABLET in 1 BOTTLE (65862-102-30)
65862-102-90 65862-102 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20070717 N/A ANDA ANDA078021 Aurobindo Pharma Limited AMLODIPINE BESYLATE 5 mg/1 90 TABLET in 1 BOTTLE (65862-102-90)
65862-102-99 65862-102 HUMAN PRESCRIPTION DRUG Amlodipine Besylate Amlodipine Besylate TABLET ORAL 20070717 N/A ANDA ANDA078021 Aurobindo Pharma Limited AMLODIPINE BESYLATE 5 mg/1 1000 TABLET in 1 BOTTLE (65862-102-99)
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