PMDA drug package insert
ディナゲスト錠1mg
PMDA Prescription drug · 持田製薬株式会社 · package insert Oct 22, 2025
Key facts
| Brand names | ディナゲスト錠1mg |
|---|---|
| Nonproprietary names | ジエノゲスト |
| Companies | 製造販売元／持田製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 子宮内膜症治療剤・子宮腺筋症に伴う疼痛改善治療剤 |
| Therapeutic category codes | 872499 |
| YJ codes | 2499010F1023 |
| Approval numbers | 21900AMX01752000 |
| Package insert edition | 第4版 |
| Package insert date | Oct 22, 2025 |
| PMDA document key | 790005_2499010F1023_1 |
| PMDA company code | 790005 |
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: