PMDA drug package insert
レミニール錠4mg
PMDA Prescription drug · 太陽ファルマ株式会社 · package insert Jun 23, 2025
Key facts
| Brand names | レミニール錠4mg, レミニール錠8mg, レミニール錠12mg, レミニールOD錠4mg, レミニールOD錠8mg, レミニールOD錠12mg, レミニール内用液4mg/mL |
|---|---|
| Nonproprietary names | ガランタミン臭化水素酸塩 |
| Companies | 製造販売元／太陽ファルマ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | アルツハイマー型認知症治療剤 |
| Therapeutic category codes | 87119 |
| YJ codes | 1190019F1028, 1190019F2024, 1190019F3020, 1190019F4027, 1190019F5023, 1190019F6020, 1190019S1026 |
| Approval numbers | 22300AMX00426000, 22300AMX00427000, 22300AMX00428000, 22300AMX00429000, 22300AMX00430000, 22300AMX00431000, 22300AMX00432000 |
| Package insert edition | 第4版 |
| Package insert date | Jun 23, 2025 |
| PMDA document key | 431010_1190019F1028_3 |
| PMDA company code | 431010 |
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: