PMDA drug package insert
オルメサルタン錠5mg「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 | オルメサルタン錠5mg「ケミファ」, オルメサルタン錠10mg「ケミファ」, オルメサルタン錠20mg「ケミファ」, オルメサルタン錠40mg「ケミファ」 |
|---|---|
| Nonproprietary names | オルメサルタン メドキソミル |
| Companies | 製造販売元／日本ケミファ株式会社, 販売元／日本薬品工業株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 高親和性AT1レセプターブロッカー |
| Therapeutic category codes | 872149 |
| YJ codes | 2149044F3108, 2149044F1091, 2149044F2098, 2149044F4104 |
| Approval numbers | 22900AMX00658000, 22900AMX00659000, 22900AMX00660000, 22900AMX00661000 |
| Package insert edition | 第2版 |
| Package insert date | Sep 9, 2025 |
| PMDA document key | 530213_2149044F1091_2 |
| 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: