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=ANDA208392"
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
25021-244-10 25021-244 HUMAN PRESCRIPTION DRUG BORTEZOMIB BORTEZOMIB INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS; SUBCUTANEOUS 20220501 N/A ANDA ANDA208392 Sagent Pharmaceuticals BORTEZOMIB 3.5 mg/1 1 VIAL in 1 CARTON (25021-244-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
51817-586-01 51817-586 HUMAN PRESCRIPTION DRUG Bortezomib bortezomib INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS; SUBCUTANEOUS 20220502 N/A ANDA ANDA208392 Pharmascience Inc. BORTEZOMIB 3.5 mg/1 1 VIAL in 1 CARTON (51817-586-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
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