- 適應症
-
- 劑型
-
- 包裝
- 詳如仿單標籤核定本。註銷規格:LK110S,LK113S,LK116S,LK119S,LK122S,LK125S,LK129S,LK132S,LK135S,LK138S,LK141S,LK145S,LK150S,LK157S,LK163S,LK175S,LK189S,LK200S,LK210S,LK213S,LK216S,LK219S,LK222S,LK225S,LK229S,LK232S,LK235S,LK238S,LK241S,LK245S,LK250S,LK257S,LK263S,LK275S,LK289S,LK300S,LA705S,LA706S,LA707S,LA708S,LA709S,LK500S,LK508S,LK510S,LK512S。規格變更:由 LB6S, LB7S, LB8S, LB9S, LB10S, LB11S, LB12S, LB14S, LB16S, LB18S, LB20S, LB26S, LB28S, LB30S, LB32S, LB34S, LB36S, LB38S, LB40S, LB41S, LB42S, LB43S, LB44S, LB45S, LB46S, LB47S, LB48S, LB49S, LB50S, LB52S, LB54S, LB56S, LB57S, LB58S, LB59S, LB60S, LB61S, LB62S, LB63S, LB64S, LB66S, LB68S, LB70S, LB72S, LB76S, LB80S, LB85S, LB90S, LB95S變更為LB006S,LB007S,LB008S, LB009S, LB010S, LB011S, LB012S, LB014S, LB016S,LB018S, LB020S,LB026S, LB028S, LB030S, LB032S, LB034S,LB036S, LB038S, LB040S, LB041S, LB042S, LB043S, LB044S,LB045S, LB046S, LB047S, LB048S, LB049S, LB050S,LB052S,LB054S, LB056S, LB057S, LB058S, LB059S, LB060S, LB061S,LB062S, LB063S, LB064S, LB066S, LB068S, LB070S, LB072S,LB076S, LB080S,LB085S, LB090S, LB095S,以下空白。
- 許可證字號
-
衛部藥製字第005945號
- 註銷狀態
- 1
- 註銷日期
-
2022-07-15
- 註銷理由
- 851
- 有效日期
-
2018-08-22
- 發證日期
-
1990-06-15
- 許可證種類
- 09
- 中文品名
- 骨釘
- 英文品名
- "AESCULAP" BONE SCREW
- 藥品類別
- 0302 人工骨螺絲
- 申請商地址
- 台北市松山區健康路152號9樓
- 通關簽審文件編號
- DHA00600594504
- 資料更新時間
-