PMDA drug package insert
デスモプレシン静注4µg「フェリング」
PMDA Prescription drug · フェリング・ファーマ株式会社 · package insert Apr 8, 2025
Key facts
| Brand names | デスモプレシン静注4µg「フェリング」 |
|---|---|
| Nonproprietary names | デスモプレシン酢酸塩水和物 |
| Companies | 製造販売元（輸入）／フェリング・ファーマ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 第Ⅷ因子放出型 血友病A・von Willebrand病用剤 |
| Therapeutic category codes | 872419 |
| YJ codes | 2419400A1032 |
| Approval numbers | 30300AMX00314 |
| Package insert edition | 第5版 |
| Package insert date | Apr 8, 2025 |
| PMDA document key | 670666_2419400A1032_1 |
| PMDA company code | 670666 |
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: