PMDA drug package insert
オキファスト注10mg
PMDA Prescription drug · シオノギファーマ株式会社 · package insert Mar 17, 2026
Key facts
| Brand names | オキファスト注10mg, オキファスト注50mg |
|---|---|
| Nonproprietary names | オキシコドン塩酸塩水和物 |
| Companies | 製造販売元／シオノギファーマ株式会社, 販売元／塩野義製薬株式会社, 提携／ムンディファーマ B.V. |
| Product type | Prescription drug |
| Therapeutic category | がん疼痛治療用注射剤 |
| Therapeutic category codes | 878119 |
| YJ codes | 8119400A1025, 8119400A2021 |
| Approval numbers | 22400AMX00025000, 22400AMX00026000 |
| Package insert edition | 第4版 |
| Package insert date | Mar 17, 2026 |
| PMDA document key | 343018_8119400A1025_2 |
| PMDA company code | 343018 |
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: