PMDA drug package insert
東洋の人参湯エキス顆粒
PMDA OTC drug · 日邦薬品工業株式会社 · package insert Jul 31, 2020
Key facts
| Brand names | 東洋の人参湯エキス顆粒 |
|---|---|
| Companies | 製造販売元／東洋漢方製薬（株）,販売会社／日邦薬品工業株式会社 |
| Product type | OTC drug |
| OTC risk class | 第２類医薬品 |
| OTC dosage form | 散剤 |
| OTC effect category | 人参湯（理中丸） |
| Package insert date | Jul 31, 2020 |
| PMDA document key | 480188_J0601010299 |
| PMDA company code | 480188 |
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: