PMDA drug package insert
ドネペジル塩酸塩OD錠3mg「テバ」
PMDA Prescription drug · T'sファーマ株式会社 · package insert Sep 1, 2025
Key facts
| Brand names | ドネペジル塩酸塩OD錠3mg「テバ」, ドネペジル塩酸塩OD錠5mg「テバ」, ドネペジル塩酸塩OD錠10mg「テバ」 |
|---|---|
| Nonproprietary names | ドネペジル塩酸塩 |
| Companies | 製造販売元／T'sファーマ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | アルツハイマー型、レビー小体型認知症治療剤 |
| Therapeutic category codes | 87119 |
| YJ codes | 1190012F3320, 1190012F4327, 1190012F6230 |
| Approval numbers | 22500AMX01393, 22500AMX01394, 22500AMX01483 |
| Package insert edition | 第4版 |
| Package insert date | Sep 1, 2025 |
| PMDA document key | 400813_1190012F3320_1 |
| PMDA company code | 400813 |
At a glance
- 1–9 Package insert revisions
- 10–99 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: