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โซฟราบิน 1000

SOFRABIN 1000

activeLast updated: 2026-07-29

Product & certifications 1

  • FDA 1C39/68(NG)drugคงอยู่

ตัวยาสำคัญ

  • GEMCITABINE HYDROCHLORIDE1139 milligramต่อ 1 vial
ประเภทควบคุม
ยาควบคุมพิเศษ
ข้อบ่งใช้
Gemcitabine is indicated for the treatment of locally advanced or metastatic bladder cancer in combination with cisplatin. Gemcitabine is indicated for treatment of patients with locally advanced or metastatic adenocarcinoma of the pancreas. Gemcitabine in combination with cisplatin is indicated as first line treatment of patients with locally advanced or metastatic non-small cell lung cancer (NSCLC). Gemcitabine monotherapy can be considered in elderly patients or those with performance status 2. Gemcitabine is indicated for the treatment of patients with locally advanced or metastatic epithelial ovarian carcinoma, in combination with carboplatin, in patients with relapsed disease following a recurrence-free interval of at least 6 months after platients with relapsed disease following a recurrence-free interval of at least 6 months after platinum-based, first-line therapy. Gemcitabine in combination with paclitaxel, is indicated for the treatment of patients with unresectable,locally recurrent or metastatic breast cancer who have relapsed following adjuvant/neoadjuvant chemotherapy. Prior chemotherapy have included an anthracycline unless clinically contraindicated.
รหัส ATC
L01BC05 (gemcitabine)

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Trade name
Juristic registration number
0105565135868

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Last updated: 2026-07-29 · Data aggregated from official government databases: NBTC · FDA · TISI · DBD · Dept. of Tourism · ACFSReport incorrect data

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