PMDA drug package insert
牛蟾参
PMDA OTC drug · ゼネル薬品工業(株) · package insert Jun 29, 2018
Key facts
| Brand names | 牛蟾参 |
|---|---|
| Companies | 製造販売元／三星製薬（株）,販売会社／（株）大心中井薬品,販売会社／（株）中京医薬品,販売会社／ゼネル薬品工業(株) |
| Product type | OTC drug |
| OTC risk class | 第２類医薬品 |
| OTC dosage form | カプセル |
| OTC effect category | 強心薬（センソ含有製剤等） |
| Package insert date | Jun 29, 2018 |
| PMDA document key | 750318_J1101000236 |
| 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: