PMDA drug package insert
アクイプタ錠60mg
PMDA Prescription drug · アッヴィ合同会社 · package insert Apr 15, 2026
Key facts
| Brand names | アクイプタ錠60mg, アクイプタ錠30mg, アクイプタ錠10mg |
|---|---|
| Nonproprietary names | アトゲパント水和物 |
| Companies | 製造販売元／アッヴィ合同会社 |
| Product type | Prescription drug |
| Therapeutic category | 経口CGRP受容体拮抗薬 |
| Therapeutic category codes | 87119 |
| YJ codes | 1190036F3024, 1190036F2028, 1190036F1021 |
| Approval numbers | 30800AMX00075000, 30800AMX00074000, 30800AMX00073000 |
| Package insert edition | 第1版 |
| Package insert date | Apr 15, 2026 |
| PMDA document key | 112130_1190036F3024_1 |
| PMDA company code | 112130 |
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: