PMDA drug package insert
スージャヌ配合錠
PMDA Prescription drug · MSD株式会社 · package insert Oct 22, 2025
Key facts
| Brand names | スージャヌ配合錠 |
|---|---|
| Nonproprietary names | シタグリプチンリン酸塩水和物・イプラグリフロジン Ｌ－プロリン配合剤 |
| Companies | 製造販売元／MSD株式会社, 発売元／アステラス製薬株式会社, 販売提携／寿製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 選択的DPP-4阻害剤／選択的SGLT2阻害剤配合剤; ◎2型糖尿病治療剤◎ |
| Therapeutic category codes | 873969 |
| YJ codes | 3969107F1022 |
| Approval numbers | 23000AMX00452000 |
| Package insert edition | 第7版 |
| Package insert date | Oct 22, 2025 |
| PMDA document key | 170050_3969107F1022_1 |
| PMDA company code | 170050 |
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: