PMDA drug package insert
カンフル精
PMDA Prescription drug · 東海製薬株式会社 · package insert Aug 7, 2023
Key facts
| Brand names | カンフル精 |
|---|---|
| Nonproprietary names | カンフル |
| Companies | 発売元／東海製薬株式会社, 製造販売元／山善製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 鎮痛・鎮痒・消炎剤 |
| Therapeutic category codes | 872645 |
| YJ codes | 2645700Q1109 |
| Approval numbers | 14600AMZ02359000 |
| Package insert edition | 第1版 |
| Package insert date | Aug 7, 2023 |
| PMDA document key | 800084_2645700Q1109_4 |
| PMDA company code | 800084 |
At a glance
- 1–9 Package insert revisions
- None 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: