PMDA drug package insert
ボラニゴ錠10mg
PMDA Prescription drug · 日本セルヴィエ株式会社 · package insert Apr 1, 2026
Key facts
| Brand names | ボラニゴ錠10mg, ボラニゴ錠40mg |
|---|---|
| Nonproprietary names | ボラシデニブ クエン酸水和物 |
| Companies | 製造販売業者等／日本セルヴィエ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 抗悪性腫瘍剤 |
| Therapeutic category codes | 87429 |
| YJ codes | 4291097F1024, 42910J1F2024 |
| Approval numbers | 30700AMX00228000, 30700AMX00229000 |
| Package insert edition | 第3版 |
| Package insert date | Apr 1, 2026 |
| PMDA document key | 530457_4291097F1024_1 |
| PMDA company code | 530457 |
At a glance
- 1–9 Package insert revisions
- 1–9 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: