PMDA drug package insert
ミラペックスLA錠0.375mg
PMDA Prescription drug · 日本ベーリンガーインゲルハイム株式会社 · package insert May 23, 2024
Key facts
| Brand names | ミラペックスLA錠0.375mg, ミラペックスLA錠1.5mg |
|---|---|
| Nonproprietary names | プラミペキソール塩酸塩水和物 |
| Companies | 製造販売元／日本ベーリンガーインゲルハイム株式会社 |
| Product type | Prescription drug |
| Therapeutic category | ドパミン作動性パーキンソン病治療徐放性製剤 |
| Therapeutic category codes | 871169 |
| YJ codes | 1169012G1028, 1169012G2024 |
| Approval numbers | 22300AMX00541000, 22300AMX00542000 |
| Package insert edition | 第3版 |
| Package insert date | May 23, 2024 |
| PMDA document key | 650168_1169012G1028_1 |
| PMDA company code | 650168 |
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: