PMDA drug package insert
デタントール錠0.5mg
PMDA Prescription drug · エーザイ株式会社 · package insert Oct 17, 2022
Key facts
| Brand names | デタントール錠0.5mg, デタントール錠1mg |
|---|---|
| Nonproprietary names | ブナゾシン塩酸塩 |
| Companies | 製造販売元／エーザイ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 血管緊張緩和・血圧降下剤 |
| Therapeutic category codes | 872149 |
| YJ codes | 2149015F1028, 2149015F2024 |
| Approval numbers | 16000AMZ00600000, 16000AMZ00601000 |
| Package insert edition | 第1版 |
| Package insert date | Oct 17, 2022 |
| PMDA document key | 170033_2149015F1028_1 |
| PMDA company code | 170033 |
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: