PMDA drug package insert
ニュベクオ錠300mg
PMDA Prescription drug · バイエル薬品株式会社 · package insert Mar 23, 2026
Key facts
| Brand names | ニュベクオ錠300mg |
|---|---|
| Nonproprietary names | ダロルタミド |
| Companies | 製造販売元／バイエル薬品株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 抗悪性腫瘍剤/アンドロゲン受容体阻害剤 |
| Therapeutic category codes | 874291 |
| YJ codes | 4291063F1025 |
| Approval numbers | 30200AMX00029000 |
| Package insert edition | 第7版 |
| Package insert date | Mar 23, 2026 |
| PMDA document key | 630004_4291063F1025_1 |
| PMDA company code | 630004 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- None 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: