PMDA drug package insert
日本薬局方 ホウ酸
PMDA OTC drug · 大洋製薬株式会社 · package insert Jun 3, 2009
Key facts
| Brand names | 日本薬局方 ホウ酸 |
|---|---|
| Companies | 製造販売元／小堺製薬株式会社,販売会社／大洋製薬株式会社 |
| Product type | OTC drug |
| OTC risk class | 第３類医薬品 |
| OTC dosage form | 散剤 |
| OTC effect category | 洗眼薬 |
| Package insert date | Jun 3, 2009 |
| PMDA document key | 270108_K0904000025 |
| PMDA company code | 270108 |
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: