PMDA drug package insert
イコサペント酸エチルカプセル300mg「BMD」
PMDA Prescription drug · 株式会社ビオメディクス · package insert Nov 13, 2024
Key facts
| Brand names | イコサペント酸エチルカプセル300mg「BMD」 |
|---|---|
| Nonproprietary names | イコサペント酸エチル |
| Companies | 製造販売元／株式会社ビオメディクス |
| Product type | Prescription drug |
| Therapeutic category | EPA製剤 |
| Therapeutic category codes | 873399872189 |
| YJ codes | 3399004M1441 |
| Approval numbers | 22500AMX01184 |
| Package insert edition | 第2版 |
| Package insert date | Nov 13, 2024 |
| PMDA document key | 650208_3399004M1441_1 |
| PMDA company code | 650208 |
At a glance
- 1–9 Package insert revisions
- 1–9 Related PMDA documents
- None 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: