PMDA drug package insert
リポバス錠5
PMDA Prescription drug · オルガノン株式会社 · package insert Sep 29, 2026
Key facts
| Brand names | リポバス錠5, リポバス錠10, リポバス錠20 |
|---|---|
| Nonproprietary names | シンバスタチン |
| Companies | 製造販売元／オルガノン株式会社 |
| Product type | Prescription drug |
| Therapeutic category | HMG-CoA還元酵素阻害剤; ◎高脂血症治療剤◎ |
| Therapeutic category codes | 872189 |
| YJ codes | 2189011F1025, 2189011F2021, 2189011F3028 |
| Approval numbers | 20300AMZ00735000, 21300AMZ00847000, 21300AMZ00848000 |
| Package insert edition | 第7版 |
| Package insert date | Sep 29, 2026 |
| PMDA document key | 181615_2189011F1025_3 |
| PMDA company code | 181615 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- None 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: