PMDA drug package insert
ソリューゲンF注
PMDA Prescription drug · 光製薬株式会社 · package insert Dec 10, 2025
Key facts
| Brand names | ソリューゲンF注 |
|---|---|
| Nonproprietary names | 酢酸リンゲル液 |
| Companies | 製造販売元／光製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 酢酸リンゲル液 |
| Therapeutic category codes | 873319 |
| YJ codes | 3319557A1030, 3319557A2060 |
| Approval numbers | 20800AMZ00386 |
| Package insert edition | 第3版 |
| Package insert date | Dec 10, 2025 |
| PMDA document key | 650014_3319557A2060_4 |
| PMDA company code | 650014 |
At a glance
- 1–9 Package insert revisions
- 1–9 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: