PMDA drug package insert
三光丸かぜぐすりカプセル
PMDA OTC drug · （株）三光丸 · package insert Sep 12, 2024
Key facts
| Brand names | 三光丸かぜぐすりカプセル |
|---|---|
| Companies | 製造販売元／寧薬化学工業（株）,販売会社／（株）三光丸 |
| Product type | OTC drug |
| OTC risk class | 第「２」類医薬品 |
| OTC dosage form | カプセル |
| OTC effect category | かぜ薬（内用） |
| Package insert date | Sep 12, 2024 |
| PMDA document key | 610001_J1501000124 |
| PMDA company code | 610001 |
At a glance
- 1–9 Package insert revisions
- 1–9 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: