N06AA04 clomipramine

NERVOUS SYSTEM PSYCHOANALEPTICS ANTIDEPRESSANTS Non-selective monoamine reuptake inhibitors

健保收載品項 TFDA 在效許可證 5 FDA 已核准

台灣藥品與外觀

台灣食藥署在效西藥許可證 5 張;以下列出 3 個品項(1 項有外觀照)。

健保收載品名:"強生"可使寧膜衣錠25毫克、"瑞士" 可必安膜衣錠25毫克(可洛米普明)、"約克"克爾鬱膠囊25毫克(可洛米普明)、〝新東〞可欣喜錠25公絲、伏憂糖衣錠25公絲(可洛米普明)〝溫士頓〞、倍欣膜衣錠25公絲(可洛米普明)、可落眠錠25公絲(可洛米普明)、安納福寧10公絲糖衣錠、安納福寧25公絲糖衣錠、解夏寧膠囊25公絲(可洛米普明)、解鬱膠囊25公絲(可洛米普明)

無外觀照
"約克"克爾鬱膠囊25毫克(可洛米普明)
"瑞士" 可必安膜衣錠25毫克(可洛米普明) 外觀
"瑞士" 可必安膜衣錠25毫克(可洛米普明)
圓形 · 白 · 刻痕:無 · 6 mm
無外觀照
"強生"可使寧膜衣錠25毫克

資料來源:食藥署「西藥許可證」+「藥品 ATC 碼」+「藥品外觀」+「藥品仿單或外盒」開放資料。外觀照與仿單連結指向食藥署原始檔。

適應症

台灣 TFDA 核准適應症

  1. 憂鬱病。
  2. 憂鬱症。

美國 FDA 適應症(英文原文對照)

美國 FDA 核准成分 clomipramine hydrochloride (商品名 CLOMIPRAMINE HYDROCHLORIDE / Clomipramine hydrochloride) · 仿單更新 2025-05-13

INDICATIONS AND USAGE Clomipramine hydrochloride capsules, USP is indicated for the treatment of obsessions and compulsions in patients with Obsessive-Compulsive Disorder (OCD). The obsessions or compulsions must cause marked distress, be time-consuming, or significantly interfere with social or occupational functioning, in order to meet the DSM-III-R (circa 1989) diagnosis of OCD. Obsessions are recurrent, persistent ideas, thoughts, images, or impulses that are ego­-dystonic. Compulsions are repetitive, purposeful, and intentional behaviors performed in response to an obsession or in a stereotyped fashion, and are recognized by the person as excessive or unreasonable. The effectiveness of clomipramine hydrochloride capsules, USP for the treatment of OCD was demonstrated in multicenter, placebo-controlled, parallel-group studies, including two 10-week studies in adults and one 8-week study in children and adolescents 10 to 17 years of age. Patients in all studies had moderate-to-severe OCD (DSM-III), with mean baseline ratings on the Yale-Brown Obsessive Compulsive Scale (YBOCS) ranging from 26 to 28 and a mean baseline rating of 10 on the NIMH Clinical Global Obsessive Compulsive Scale (NIMH-OC). Patients taking CMI experienced a mean reduction of approximately 10 on the YBOCS, representing an average improvement on this scale of 35% to 42% among adults and 37% among children and adolescents. CMI-treated patients experienced a 3.5 unit decrement on the NIMH-OC. Patients on placebo showed no important clinical response on either scale. The maximum dose was 250 mg/day for most adults and 3 mg/kg/day (up to 200 mg) for all children and adolescents. The effectiveness of clomipramine hydrochloride capsules, USP for long-term use (i.e., for more than 10 weeks) has not been systematically evaluated in placebo-controlled trials. The physician who elects to use clomipramine hydrochloride capsules, USP for extended periods should periodically reevaluate the long-term usefulness of the drug for the individual patient ( see DOSAGE AND ADMINISTRATION ).

資料來源:食藥署西藥許可證適應症(中文)、openFDA US SPL(英文,僅供對照)。

健保給付規定

查無健保特殊給付規定條款;本藥品依一般健保藥品支付規定給付。

實證補充

本藥品尚無實證補充整理(未來新增 Review/指引知識時補列)。


台灣藥品與適應症:食藥署西藥許可證+ATC+外觀+仿單開放資料 · FDA:openFDA US SPL · 健保給付:健保署「全民健康保險藥品給付規定」(更新日 2026-06-09)· 實證補充:人工彙整。 本頁為資訊整理,實際給付與適應症以主管機關公告為準。