PMDA drug package insert
フェルビナクパップ70mg「東光」
PMDA Prescription drug · 東光薬品工業株式会社 · package insert Oct 8, 2024
Key facts
| Brand names | フェルビナクパップ70mg「東光」, フェルビナクパップ140mg「東光」 |
|---|---|
| Nonproprietary names | フェルビナク |
| Companies | 製造販売元／東光薬品工業株式会社, 販売元／日本ジェネリック株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 経皮鎮痛消炎パップ剤 |
| Therapeutic category codes | 872649 |
| YJ codes | 2649731S1275, 2649731S3065 |
| Approval numbers | 22600AMX00893000, 22600AMX00896000 |
| Package insert edition | 第3版 |
| Package insert date | Oct 8, 2024 |
| PMDA document key | 480114_2649731S1275_2 |
| 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: