PMDA drug package insert
ウエキクス錠5mg
PMDA Prescription drug · ヴィアトリス製薬合同会社 · package insert Sep 16, 2026
Key facts
| Brand names | ウエキクス錠5mg, ウエキクス錠20mg |
|---|---|
| Nonproprietary names | ピトリサント塩酸塩 |
| Companies | 製造販売元／ヴィアトリス製薬合同会社 |
| Product type | Prescription drug |
| Therapeutic category | ヒスタミンH3受容体拮抗薬・逆作動薬 |
| Therapeutic category codes | 871179 |
| YJ codes | 11790C6F1024, 11790C6F2020 |
| Approval numbers | 30800AMX00338, 30800AMX00339 |
| Package insert edition | 第1版 |
| Package insert date | Sep 16, 2026 |
| PMDA document key | 671450_11790C6F1024_1 |
| PMDA company code | 671450 |
At a glance
- 1–9 Package insert revisions
- 1–9 Related PMDA documents
- None Safety communications
- No 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: