PMDA drug package insert
トリセノックス点滴静注12mg
PMDA Prescription drug · 日本新薬株式会社 · package insert Nov 21, 2023
Key facts
| Brand names | トリセノックス点滴静注12mg |
|---|---|
| Nonproprietary names | 三酸化二ヒ素 |
| Companies | 製造販売元／日本新薬株式会社, 提携／Teva Pharmaceutical Industries Ltd. |
| Product type | Prescription drug |
| Therapeutic category | 再発・難治性急性前骨髄球性白血病治療剤 |
| Therapeutic category codes | 874291 |
| YJ codes | 4291409A2022 |
| Approval numbers | 30400AMX00116000 |
| Package insert edition | 第2版 |
| Package insert date | Nov 21, 2023 |
| PMDA document key | 530263_4291409A2022_1 |
| PMDA company code | 530263 |
At a glance
- 1–9 Package insert revisions
- 1–9 Related PMDA documents
- None Safety communications
- No PMDA review report published
- No Risk management plan (RMP)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMDA approved drugs and package inserts (Japan)
Japan's PMDA publishes the package insert (添付文書) of every prescription drug, OTC drug and regenerative medical product, with brand and nonproprietary names, YJ codes and approval numbers. Names appear in Japanese as published.
Source: Pharmaceuticals and Medical Devices Agency (PMDA), Japan, package insert database · Source date: