常盈促腎上腺皮質素放射免疫分析法
DSL ACTH RIA

適應症
利用放射性免疫定量方法檢測血漿中的促腎上腺皮質素。  
劑型
 
包裝
DSL-2300: 100 tubes 
許可證字號
衛部藥製字第015918號 
註銷狀態
1 
註銷日期
2012-11-26  
註銷理由
838 
有效日期
2011-01-23  
發證日期
2006-01-23  
許可證種類
09 
中文品名
常盈促腎上腺皮質素放射免疫分析法 
英文品名
DSL ACTH RIA 
藥品類別
A 臨床化學及臨床毒理學 
申請商名稱
常盈實業股份有限公司  
申請商地址
台北市北投區永興路一段49號 
通關簽審文件編號
DHAS0601591802 
資料更新時間
 
製造商
名稱 廠址 公司地址 國別 製程
DIAGNOSTIC SYSTEMS LABORATORIES, INC. 445 MEDICAL CENTER BOULEVARD WEBSTER, TEXAS 77598 U.S.A. US
成份表
處方標示 成分名稱 含量 單位
1 A. ACTH Standards: (Lyophilized) One vial, labeled A, containing 0 pg/mL and five vials, labeled B-F, containing concentrations of approximately 25, 100, 200, 500 and 1000 pg/mL (5.5 -220.0 pmol/L) ACTH in a protein-based buffer with sodium azide as a preservative. Refer to vial labels for exact concentrations. Store unopened at 2-8°C until expiration date. Reconstitute Standard A with 5 mL of ACTH Buffer. Reconstitute Standards B-F with 1 mL of ACTH Assay Buffer. Use immediately upon reconstitution. Discard after use. STANDARDIZATION NOTE: The ACTH Standards & Controls have been calibrated to the World Health Organization International Reference Reagent for ACTH (code 74/555) and performance verified by immunoassay. B. ACTH [I-125] Reagent: (Lyophilized) (RED) One vial, containing < 5 μCi (185 kBq) of [I-125]-labeled ACTH in a buffer with a protein stabilizer and sodium azide as a preservative. Store unopened at 2-8°C until expiration date. Reconstitute with 11 mL ACTH Assay Buffer. Use immediately upon reco