PMDA drug package insert
ジオン注生食液付
PMDA Prescription drug · ジェイドルフ製薬株式会社 · package insert Mar 5, 2026
Key facts
| Brand names | ジオン注生食液付 |
|---|---|
| Nonproprietary names | 硫酸アルミニウムカリウム水和物・タンニン酸 |
| Companies | 製造販売元／ジェイドルフ製薬株式会社, 提携先／レキオファーマ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 内痔核硬化療法剤 |
| Therapeutic category codes | 872559 |
| YJ codes | 2559500A2020 |
| Approval numbers | 21600AMZ00517 |
| Package insert edition | 第3版 |
| Package insert date | Mar 5, 2026 |
| PMDA document key | 340269_2559500A2020_3 |
| PMDA company code | 340269 |
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: