PMDA drug package insert
アイノフロー吸入用800ppm
PMDA Prescription drug · エア・ウォーター・メディカル株式会社 · package insert Apr 21, 2026
Key facts
| Brand names | アイノフロー吸入用800ppm, アイノフロー吸入用4,880ppm EVO |
|---|---|
| Nonproprietary names | 一酸化窒素 |
| Companies | 選任外国製造医薬品等製造販売業者／エア・ウォーター・メディカル株式会社, 外国製造医薬品等特例承認取得者／マリンクロット マニュファクチュアリング エルエルシー（米国）, 製造（輸入）業者／住友精化株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 肺血管拡張剤（吸入用ガス） |
| Therapeutic category codes | 872190 |
| YJ codes | 2190700G1020, 2190700G2027 |
| Approval numbers | 22000AMI00004000, 30800AMI00001000 |
| Package insert edition | 第3版 |
| Package insert date | Apr 21, 2026 |
| PMDA document key | 130017_2190700G1020_2 |
| PMDA company code | 130017 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- None Safety communications
- Yes PMDA review report published
- Yes 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: