PMDA drug package insert
イルベサルタン錠50mg「ケミファ」
PMDA Prescription drug · 日本ケミファ株式会社 · package insert Sep 9, 2025
Key facts
| Brand names | イルベサルタン錠50mg「ケミファ」, イルベサルタン錠100mg「ケミファ」, イルベサルタン錠200mg「ケミファ」 |
|---|---|
| Nonproprietary names | イルベサルタン |
| Companies | 製造販売元／日本ケミファ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 長時間作用型ARB |
| Therapeutic category codes | 872149 |
| YJ codes | 2149046F1090, 2149046F2097, 2149046F3093 |
| Approval numbers | 22900AMX00705000, 22900AMX00706000, 22900AMX00707000 |
| Package insert edition | 第4版 |
| Package insert date | Sep 9, 2025 |
| PMDA document key | 530213_2149046F1090_1 |
| PMDA company code | 530213 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- 1–9 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: