PMDA drug package insert
ユリス錠0.5mg
PMDA Prescription drug · 持田製薬株式会社 · package insert Jul 1, 2026
Key facts
| Brand names | ユリス錠0.5mg, ユリス錠1mg, ユリス錠2mg |
|---|---|
| Nonproprietary names | ドチヌラド |
| Companies | 製造販売元／持田製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 選択的尿酸再吸収阻害薬; 高尿酸血症治療剤 |
| Therapeutic category codes | 873949 |
| YJ codes | 3949005F1022, 3949005F2029, 3949005F3025 |
| Approval numbers | 30200AMX00020000, 30200AMX00021000, 30200AMX00022000 |
| Package insert edition | 第7版 |
| Package insert date | Jul 1, 2026 |
| PMDA document key | 790005_3949005F1022_2 |
| PMDA company code | 790005 |
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: