PMDA drug package insert
テラポニンのどスプレー
PMDA OTC drug · 福地製薬（株） · package insert Nov 21, 2007
Key facts
| Brand names | テラポニンのどスプレー |
|---|---|
| Companies | 製造販売元／福地製薬（株） |
| Product type | OTC drug |
| OTC risk class | 第３類医薬品 |
| OTC dosage form | 噴霧剤 |
| OTC effect category | 口腔咽喉薬（せき，たんを標榜しないトローチ剤を含む） |
| Package insert date | Nov 21, 2007 |
| PMDA document key | 670055_J0601008402 |
| PMDA company code | 670055 |
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: