PMDA drug package insert
イーケプラ錠250mg
PMDA Prescription drug · ユーシービージャパン株式会社 · package insert Mar 17, 2026
Key facts
| Brand names | イーケプラ錠250mg, イーケプラ錠500mg |
|---|---|
| Nonproprietary names | レベチラセタム |
| Companies | 製造販売元／ユーシービージャパン株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 抗てんかん剤 |
| Therapeutic category codes | 871139 |
| YJ codes | 1139010F1024, 1139010F2020 |
| Approval numbers | 22200AMX00864000, 22200AMX00865000 |
| Package insert edition | 第6版 |
| Package insert date | Mar 17, 2026 |
| PMDA document key | 820110_1139010F1024_1 |
| PMDA company code | 820110 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- 1–9 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: