PMDA drug package insert
イムデトラ点滴静注用1mg
PMDA Prescription drug · アムジェン株式会社 · package insert May 26, 2026
Key facts
| Brand names | イムデトラ点滴静注用1mg, イムデトラ点滴静注用10mg |
|---|---|
| Nonproprietary names | タルラタマブ（遺伝子組換え） |
| Companies | 製造販売元／アムジェン株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 抗悪性腫瘍剤/二重特異性タンパク製剤 |
| Therapeutic category codes | 874291 |
| YJ codes | 4291477D1029, 4291477D2025 |
| Approval numbers | 30600AMX00310000, 30600AMX00311000 |
| Package insert edition | 第6版 |
| Package insert date | May 26, 2026 |
| PMDA document key | 112292_4291477D1029_1 |
| PMDA company code | 112292 |
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: