PMDA drug package insert
セタネオ点眼液0.002%
PMDA Prescription drug · 参天製薬株式会社 · package insert Oct 23, 2025
Key facts
| Brand names | セタネオ点眼液0.002% |
|---|---|
| Nonproprietary names | セペタプロスト |
| Companies | 製造販売元／参天製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 二環式プロスタグランジン誘導体; 緑内障・高眼圧症治療剤 |
| Therapeutic category codes | 871319 |
| YJ codes | 1319766Q1026 |
| Approval numbers | 30700AMX00203 |
| Package insert edition | 第2版 |
| Package insert date | Oct 23, 2025 |
| PMDA document key | 300237_1319766Q1026_1 |
| PMDA company code | 300237 |
At a glance
- 1–9 Package insert revisions
- 1–9 Related PMDA documents
- None Safety communications
- Yes PMDA review report published
- Yes 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: