PMDA drug package insert
アルボースうがい薬CPN
PMDA OTC drug · （株）アルボース · package insert Jun 1, 2011
Key facts
| Brand names | アルボースうがい薬CPN |
|---|---|
| Companies | 製造販売元／丸石製薬（株）,販売元／（株）アルボース |
| Product type | OTC drug |
| OTC risk class | なし |
| OTC dosage form | 液剤 |
| OTC effect category | 含嗽薬 |
| Package insert date | Jun 1, 2011 |
| PMDA document key | 730119_J1101000125 |
| PMDA company code | 730119 |
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: