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=ANDA208719"
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
70771-1115-3 70771-1115 HUMAN PRESCRIPTION DRUG Doxazosin Doxazosin TABLET ORAL 20170831 N/A ANDA ANDA208719 Zydus Lifesciences Limited DOXAZOSIN MESYLATE 8 mg/1 30 TABLET in 1 BOTTLE (70771-1115-3)
70771-1115-4 70771-1115 HUMAN PRESCRIPTION DRUG Doxazosin Doxazosin TABLET ORAL 20170831 N/A ANDA ANDA208719 Zydus Lifesciences Limited DOXAZOSIN MESYLATE 8 mg/1 10 BLISTER PACK in 1 CARTON (70771-1115-4) / 10 TABLET in 1 BLISTER PACK (70771-1115-2)
70518-3965-0 70518-3965 HUMAN PRESCRIPTION DRUG Doxazosin Doxazosin TABLET ORAL 20231217 N/A ANDA ANDA208719 REMEDYREPACK INC. DOXAZOSIN MESYLATE 2 mg/1 30 TABLET in 1 BLISTER PACK (70518-3965-0)
70518-3965-1 70518-3965 HUMAN PRESCRIPTION DRUG Doxazosin Doxazosin TABLET ORAL 20240501 N/A ANDA ANDA208719 REMEDYREPACK INC. DOXAZOSIN MESYLATE 2 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (70518-3965-1)
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