PMDA drug package insert
フルイトラン錠1mg
PMDA Prescription drug · シオノギファーマ株式会社 · package insert May 20, 2025
Key facts
| Brand names | フルイトラン錠1mg, フルイトラン錠2mg |
|---|---|
| Nonproprietary names | トリクロルメチアジド |
| Companies | 製造販売元／シオノギファーマ株式会社, 販売元／塩野義製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | チアジド系降圧利尿剤 |
| Therapeutic category codes | 872132 |
| YJ codes | 2132003F3039, 2132003F1257 |
| Approval numbers | 22100AMX00343000, 13527KUY07492001 |
| Package insert edition | 第3版 |
| Package insert date | May 20, 2025 |
| PMDA document key | 343018_2132003F1257_2 |
| PMDA company code | 343018 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- None 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: