PMDA drug package insert
バンヒントDX
PMDA OTC drug · 日本医薬品製造（株） · package insert May 20, 2011
Key facts
| Brand names | バンヒントDX |
|---|---|
| Companies | 製造販売元／日本医薬品製造（株） |
| Product type | OTC drug |
| OTC risk class | 第３類医薬品 |
| OTC dosage form | 液剤 |
| OTC effect category | ビタミン含有保健薬（ビタミン剤等） |
| Package insert date | May 20, 2011 |
| PMDA document key | 530170_J0601004768 |
| PMDA company code | 530170 |
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: