PMDA drug package insert
エキザルベ
PMDA Prescription drug · マルホ株式会社 · package insert May 25, 2023
Key facts
| Brand names | エキザルベ |
|---|---|
| Nonproprietary names | 混合死菌製剤 |
| Companies | 製造販売／マルホ株式会社, 提携／ドクトル・カーデ製薬会社 |
| Product type | Prescription drug |
| Therapeutic category | 皮膚疾患治療剤 |
| Therapeutic category codes | 872649 |
| YJ codes | 2649852M1020 |
| Approval numbers | 13600AZY00423000 |
| Package insert edition | 第1版 |
| Package insert date | May 25, 2023 |
| PMDA document key | 730155_2649852M1020_1 |
| PMDA company code | 730155 |
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: