PMDA drug package insert
フルナーゼ点鼻液50μg 28噴霧用
PMDA Prescription drug · グラクソ・スミスクライン株式会社 · package insert Aug 26, 2025
Key facts
| Brand names | フルナーゼ点鼻液50μg 28噴霧用, フルナーゼ点鼻液50μg 56噴霧用 |
|---|---|
| Nonproprietary names | フルチカゾンプロピオン酸エステル |
| Companies | 製造販売元／グラクソ・スミスクライン株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 定量噴霧式鼻過敏症治療剤 |
| Therapeutic category codes | 871329 |
| YJ codes | 1329707Q1181, 1329707Q3052 |
| Approval numbers | 21900AMX00018, 21800AMY10050 |
| Package insert edition | 第2版 |
| Package insert date | Aug 26, 2025 |
| PMDA document key | 340278_1329707Q1181_1 |
| PMDA company code | 340278 |
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: