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=ANDA091041"
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
25021-466-05 25021-466 HUMAN PRESCRIPTION DRUG Octreotide Acetate octreotide acetate INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20230615 N/A ANDA ANDA091041 Sagent Pharmaceuticals OCTREOTIDE ACETATE 200 ug/mL 1 VIAL in 1 CARTON (25021-466-05) / 5 mL in 1 VIAL
25021-467-05 25021-467 HUMAN PRESCRIPTION DRUG Octreotide Acetate octreotide acetate INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20230615 N/A ANDA ANDA091041 Sagent Pharmaceuticals OCTREOTIDE ACETATE 1000 ug/mL 1 VIAL in 1 CARTON (25021-467-05) / 5 mL in 1 VIAL
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