PMDA drug package insert
アイミクス配合錠LD
PMDA Prescription drug · 住友ファーマ株式会社 · package insert Sep 9, 2025
Key facts
| Brand names | アイミクス配合錠LD, アイミクス配合錠HD |
|---|---|
| Nonproprietary names | イルベサルタン・アムロジピンベシル酸塩配合剤 |
| Companies | 製造販売元／住友ファーマ株式会社, 提携／SANOFI |
| Product type | Prescription drug |
| Therapeutic category | 長時間作用型ARB/持続性Ca拮抗薬配合剤 |
| Therapeutic category codes | 872149 |
| YJ codes | 2149118F1020, 2149118F2026 |
| Approval numbers | 22400AMX01391, 22400AMX01392 |
| Package insert edition | 第6版 |
| Package insert date | Sep 9, 2025 |
| PMDA document key | 400093_2149118F1020_1 |
| PMDA company code | 400093 |
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: