PMDA drug package insert
プロピベリン塩酸塩錠10mg「あすか」
PMDA Prescription drug · あすか製薬株式会社 · package insert Oct 31, 2024
Key facts
| Brand names | プロピベリン塩酸塩錠10mg「あすか」, プロピベリン塩酸塩錠20mg「あすか」 |
|---|---|
| Nonproprietary names | プロピベリン塩酸塩 |
| Companies | 製造販売元／あすか製薬株式会社, 販売元／武田薬品工業株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 尿失禁; 頻尿; 過活動膀胱治療剤 |
| Therapeutic category codes | 87259 |
| YJ codes | 2590007F1323, 2590007F2311 |
| Approval numbers | 23000AMX00049, 23000AMX00050 |
| Package insert edition | 第2版 |
| Package insert date | Oct 31, 2024 |
| PMDA document key | 470007_2590007F1323_1 |
| PMDA company code | 470007 |
At a glance
- 1–9 Package insert revisions
- 10–99 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: