PMDA drug package insert
ボンビバ静注1mgシリンジ
PMDA Prescription drug · 大正製薬株式会社 · package insert Oct 12, 2023
Key facts
| Brand names | ボンビバ静注1mgシリンジ |
|---|---|
| Nonproprietary names | イバンドロン酸ナトリウム水和物 |
| Companies | 製造販売／大正製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 骨粗鬆症治療剤 |
| Therapeutic category codes | 873999 |
| YJ codes | 3999438G1027 |
| Approval numbers | 22500AMX01004000 |
| Package insert edition | 第5版 |
| Package insert date | Oct 12, 2023 |
| PMDA document key | 400059_3999438G1027_3 |
| PMDA company code | 400059 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- None Safety communications
- Yes 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: