PMDA drug package insert
六神丸
PMDA OTC drug · 大草薬品(株) · package insert May 1, 2007
Key facts
| Brand names | 六神丸 |
|---|---|
| Companies | 製造販売元／三星製薬（株）,販売会社／滋賀県製薬（株）,販売会社／ワキ製薬（株）,販売会社／大昭製薬(株)，常盤薬品工業(株)，(株)やまと薬品，(株)赤玉堂,販売会社／大草薬品(株) |
| Product type | OTC drug |
| OTC risk class | 第２類医薬品 |
| OTC dosage form | 錠剤 |
| OTC effect category | 強心薬（センソ含有製剤等） |
| Package insert date | May 1, 2007 |
| PMDA document key | 750318_J0601011849 |
| PMDA company code | 750318 |
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: