PMDA drug package insert
ボンベンディ静注用1300
PMDA Prescription drug · 武田薬品工業株式会社 · package insert Feb 19, 2026
Key facts
| Brand names | ボンベンディ静注用1300 |
|---|---|
| Nonproprietary names | ボニコグ アルファ（遺伝子組換え） |
| Companies | 製造販売元／武田薬品工業株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 遺伝子組換えヒトvon Willebrand因子製剤 |
| Therapeutic category codes | 876349 |
| YJ codes | 6343455D1020 |
| Approval numbers | 30200AMX00424 |
| Package insert edition | 第7版 |
| Package insert date | Feb 19, 2026 |
| PMDA document key | 400256_6343455D1020_2 |
| PMDA company code | 400256 |
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: