PMDA drug package insert
ビソプロロールフマル酸塩錠0.625mg「ZE」
PMDA Prescription drug · 全星薬品工業株式会社 · package insert Sep 1, 2026
Key facts
| Brand names | ビソプロロールフマル酸塩錠0.625mg「ZE」, ビソプロロールフマル酸塩錠2.5mg「ZE」, ビソプロロールフマル酸塩錠5mg「ZE」 |
|---|---|
| Nonproprietary names | ビソプロロールフマル酸塩 |
| Companies | 製造販売元／全星薬品工業株式会社, 発売元／全星薬品株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 選択的β1アンタゴニスト |
| Therapeutic category codes | 872123 |
| YJ codes | 2123016F3053, 2123016F1140, 2123016F2227 |
| Approval numbers | 22500AMX01632, 22500AMX01213, 22500AMX01214 |
| Package insert edition | 第3版 |
| Package insert date | Sep 1, 2026 |
| PMDA document key | 380087_2123016F1140_1 |
| PMDA company code | 380087 |
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: