PMDA drug package insert
エスコン内服液
PMDA OTC drug · 福地製薬（株） · package insert Sep 1, 2007
Key facts
| Brand names | エスコン内服液 |
|---|---|
| Companies | 製造販売元／美吉野製薬（株）,販売会社／福地製薬（株） |
| Product type | OTC drug |
| Package insert date | Sep 1, 2007 |
| PMDA document key | 750150_J0601004394 |
| PMDA company code | 750150 |
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: