PMDA drug package insert
レクサプロ錠10mg
PMDA Prescription drug · 持田製薬株式会社 · package insert Apr 1, 2025
Key facts
| Brand names | レクサプロ錠10mg, レクサプロ錠20mg |
|---|---|
| Nonproprietary names | エスシタロプラムシュウ酸塩 |
| Companies | 製造販売元／持田製薬株式会社, 提携／Lundbeck |
| Product type | Prescription drug |
| Therapeutic category | 選択的セロトニン再取り込み阻害剤（SSRI） |
| Therapeutic category codes | 871179 |
| YJ codes | 1179054F1022, 1179054F2029 |
| Approval numbers | 22300AMX00517000, 23000AMX00835000 |
| Package insert edition | 第7版 |
| Package insert date | Apr 1, 2025 |
| PMDA document key | 790005_1179054F1022_1 |
| PMDA company code | 790005 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- 1–9 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: