PMDA drug package insert
プロスタルモン・F注射液1000
PMDA Prescription drug · 丸石製薬株式会社 · package insert Jun 16, 2026
Key facts
| Brand names | プロスタルモン・F注射液1000 |
|---|---|
| Nonproprietary names | ジノプロスト |
| Companies | 製造販売元／丸石製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | プロスタグランジンF2α製剤 |
| Therapeutic category codes | 872499 |
| YJ codes | 2499401A2050 |
| Approval numbers | 14800AMZ00036 |
| Package insert edition | 第4版 |
| Package insert date | Jun 16, 2026 |
| PMDA document key | 730119_2499401A2050_2 |
| PMDA company code | 730119 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- 10–99 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: