PMDA drug package insert
ユクリズム
PMDA OTC drug · ロート製薬（株） · package insert Sep 30, 2026
Key facts
| Brand names | ユクリズム |
|---|---|
| Companies | 製造販売元／大峰堂薬品工業（株）,販売会社／ロート製薬（株） |
| Product type | OTC drug |
| OTC risk class | 第２類医薬品 |
| OTC dosage form | 錠剤 |
| OTC effect category | 加味帰脾湯 |
| Package insert date | Sep 30, 2026 |
| PMDA document key | 180102_K1610000006 |
| PMDA company code | 180102 |
At a glance
- 1–9 Package insert revisions
- 1–9 Related PMDA documents
- 1–9 Safety communications
- No PMDA review report published
- No 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: