PMDA drug package insert
ボーンワックス
PMDA Prescription drug · 株式会社東京エム・アイ商会東京都江東区平野3丁目2番6号 · package insert Feb 1, 2024
Key facts
| Brand names | ボーンワックス |
|---|---|
| Nonproprietary names | ミツロウ |
| Companies | 製造販売元／株式会社東京エム・アイ商会東京都江東区平野3丁目2番6号 |
| Product type | Prescription drug |
| Therapeutic category | 骨髄止血剤 |
| Therapeutic category codes | 873329 |
| YJ codes | 332970AM1033 |
| Approval numbers | 13800AZY00179000 |
| Package insert date | Feb 1, 2024 |
| PMDA document key | 480053_332970AM1033_1 |
| PMDA company code | 480053 |
At a glance
- 1–9 Package insert revisions
- None Related PMDA documents
- None Safety communications
- No 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: