PMDA drug package insert
タズベリク錠200mg
PMDA Prescription drug · エーザイ株式会社 · package insert Sep 17, 2025
Key facts
| Brand names | タズベリク錠200mg |
|---|---|
| Nonproprietary names | タゼメトスタット臭化水素酸塩 |
| Companies | 製造販売元／エーザイ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 抗悪性腫瘍剤（EZH2阻害剤） |
| Therapeutic category codes | 874291 |
| YJ codes | 4291073F1029 |
| Approval numbers | 30300AMX00278000 |
| Package insert edition | 第6版 |
| Package insert date | Sep 17, 2025 |
| PMDA document key | 170033_4291073F1029_1 |
| PMDA company code | 170033 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- 1–9 Safety communications
- Yes PMDA review report published
- Yes 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: