PMDA drug package insert
ミティキュアダニ舌下錠3,300JAU
PMDA Prescription drug · 鳥居薬品株式会社 · package insert Jul 6, 2023
Key facts
| Brand names | ミティキュアダニ舌下錠3,300JAU, ミティキュアダニ舌下錠10,000JAU |
|---|---|
| Nonproprietary names | アレルゲンエキス |
| Companies | 製造販売元／鳥居薬品株式会社 |
| Product type | Prescription drug |
| Therapeutic category | ダニアレルギーの減感作療法（アレルゲン免疫療法）薬 |
| Therapeutic category codes | 87449 |
| YJ codes | 4490031F1029, 4490031F2025 |
| Approval numbers | 22700AMX01022000, 22700AMX01023000 |
| Package insert edition | 第1版 |
| Package insert date | Jul 6, 2023 |
| PMDA document key | 480306_4490031F1029_1 |
| PMDA company code | 480306 |
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: