PMDA drug package insert
レキップ錠0.25mg
PMDA Prescription drug · グラクソ・スミスクライン株式会社 · package insert Feb 24, 2026
Key facts
| Brand names | レキップ錠0.25mg, レキップ錠1mg, レキップ錠2mg |
|---|---|
| Nonproprietary names | ロピニロール塩酸塩 |
| Companies | 製造販売元／グラクソ・スミスクライン株式会社 |
| Product type | Prescription drug |
| Therapeutic category | ドパミンD2受容体系作動薬 |
| Therapeutic category codes | 871169 |
| YJ codes | 1169013F1027, 1169013F2023, 1169013F3020 |
| Approval numbers | 21800AMY10125, 21800AMY10126, 21800AMY10123 |
| Package insert edition | 第3版 |
| Package insert date | Feb 24, 2026 |
| PMDA document key | 340278_1169013F1027_1 |
| PMDA company code | 340278 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- None Safety communications
- Yes 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: