PMDA drug package insert
新サルファ・ルビー
PMDA OTC drug · 日邦薬品工業（株） · package insert Jan 7, 2025
Key facts
| Brand names | 新サルファ・ルビー |
|---|---|
| Companies | 製造販売元／牛津製薬（株）,販売会社／日邦薬品工業（株） |
| Product type | OTC drug |
| OTC risk class | 第２類医薬品 |
| OTC dosage form | 液剤 |
| OTC effect category | 抗菌性点眼薬 |
| Package insert date | Jan 7, 2025 |
| PMDA document key | 160033_J0601008053 |
| PMDA company code | 160033 |
At a glance
- 1–9 Package insert revisions
- 1–9 Related PMDA documents
- 1–9 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: