PMDA drug package insert
ケトプロフェンテープ20mg「東光」
PMDA Prescription drug · 東光薬品工業株式会社 · package insert Feb 25, 2025
Key facts
| Brand names | ケトプロフェンテープ20mg「東光」, ケトプロフェンテープ40mg「東光」 |
|---|---|
| Nonproprietary names | ケトプロフェン |
| Companies | 製造販売元／東光薬品工業株式会社, 発売元／ラクール薬品販売株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 経皮鎮痛消炎剤 |
| Therapeutic category codes | 872649 |
| YJ codes | 2649729S2215, 2649729S3149 |
| Approval numbers | 22100AMX00728000, 22100AMX00729000 |
| Package insert edition | 第2版 |
| Package insert date | Feb 25, 2025 |
| PMDA document key | 480114_2649729S2215_1 |
| PMDA company code | 480114 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- 1–9 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: