PMDA drug package insert
エフルエルダ筋注
PMDA Prescription drug · サノフィ株式会社 · package insert Dec 27, 2024
Key facts
| Brand names | エフルエルダ筋注 |
|---|---|
| Nonproprietary names | 高用量インフルエンザＨＡワクチン |
| Companies | 製造販売元／サノフィ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | ウイルスワクチン類 |
| Therapeutic category codes | 876313 |
| YJ codes | 631341RG1020 |
| Approval numbers | 30600AMX00298 |
| Package insert edition | 第1版 |
| Package insert date | Dec 27, 2024 |
| PMDA document key | 780069_631341RG1020_1 |
| PMDA company code | 780069 |
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: