PMDA drug package insert
ペメトレキセド点滴静注液100mg「トーワ」
PMDA Prescription drug · 富士フイルム富山化学株式会社 · package insert Jun 5, 2025
Key facts
| Brand names | ペメトレキセド点滴静注液100mg「トーワ」, ペメトレキセド点滴静注液500mg「トーワ」, ペメトレキセド点滴静注液800mg「トーワ」 |
|---|---|
| Nonproprietary names | ペメトレキセドナトリウムヘミペンタ水和物 |
| Companies | 製造販売元／富士フイルム富山化学株式会社, 発売／東和薬品株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 代謝拮抗性抗悪性腫瘍剤 |
| Therapeutic category codes | 874229 |
| YJ codes | 4229401A1040, 4229401A2046, 4229401A3042 |
| Approval numbers | 30300AMX00094000, 30300AMX00095000, 30600AMX00206000 |
| Package insert edition | 第7版 |
| Package insert date | Jun 5, 2025 |
| PMDA document key | 400022_4229401A1040_1 |
| PMDA company code | 400022 |
At a glance
- 1–9 Package insert revisions
- 10–99 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: