PMDA drug package insert
ラピフォートワイプ2.5%
PMDA Prescription drug · マルホ株式会社 · package insert May 1, 2023
Key facts
| Brand names | ラピフォートワイプ2.5% |
|---|---|
| Nonproprietary names | グリコピロニウムトシル酸塩水和物 |
| Companies | 製造販売／マルホ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 原発性腋窩多汗症治療剤 |
| Therapeutic category codes | 871259 |
| YJ codes | 1259701X1026 |
| Approval numbers | 30400AMX00009000 |
| Package insert edition | 第3版 |
| Package insert date | May 1, 2023 |
| PMDA document key | 730155_1259701X1026_1 |
| PMDA company code | 730155 |
At a glance
- 1–9 Package insert revisions
- 1–9 Related PMDA documents
- None Safety communications
- Yes PMDA review report published
- Yes 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: