PMDA drug package insert
ジョエンジャ錠10mg
PMDA Prescription drug · 株式会社オーファンパシフィック · package insert Aug 13, 2026
Key facts
| Brand names | ジョエンジャ錠10mg, ジョエンジャ錠30mg, ジョエンジャ錠70mg |
|---|---|
| Nonproprietary names | レニオリシブリン酸塩 |
| Companies | 製造販売元／株式会社オーファンパシフィック |
| Product type | Prescription drug |
| Therapeutic category | 活性化PI3Kδ症候群治療剤 |
| Therapeutic category codes | 873999 |
| YJ codes | 3999073F1020, 3999073F2027, 3999073F3023 |
| Approval numbers | 30800AMX00121000, 30800AMX00120000, 30800AMX00119000 |
| Package insert edition | 第2版 |
| Package insert date | Aug 13, 2026 |
| PMDA document key | 181251_3999073F1020_1 |
| PMDA company code | 181251 |
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: