PMDA drug package insert
イヌリード注
PMDA Prescription drug · 株式会社富士薬品 · package insert Dec 2, 2024
Key facts
| Brand names | イヌリード注 |
|---|---|
| Nonproprietary names | イヌリン |
| Companies | 製造販売元／株式会社富士薬品 |
| Product type | Prescription drug |
| Therapeutic category | 腎機能検査用薬 |
| Therapeutic category codes | 877225 |
| YJ codes | 7225403A2023 |
| Approval numbers | 21700AMZ00748000 |
| Package insert edition | 第2版 |
| Package insert date | Dec 2, 2024 |
| PMDA document key | 670242_7225403A2023_1 |
| PMDA company code | 670242 |
At a glance
- 1–9 Package insert revisions
- 1–9 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: