PMDA drug package insert
セディール錠5mg
PMDA Prescription drug · 住友ファーマ株式会社 · package insert Mar 2, 2026
Key facts
| Brand names | セディール錠5mg, セディール錠10mg, セディール錠20mg |
|---|---|
| Nonproprietary names | タンドスピロンクエン酸塩 |
| Companies | 製造販売元／住友ファーマ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | セロトニン作動性抗不安薬 |
| Therapeutic category codes | 871129 |
| YJ codes | 1129008F1039, 1129008F2035, 1129008F3023 |
| Approval numbers | 21900AMX00163, 21900AMX00164, 21800AMZ10325 |
| Package insert edition | 第2版 |
| Package insert date | Mar 2, 2026 |
| PMDA document key | 400093_1129008F1039_2 |
| PMDA company code | 400093 |
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: