PMDA drug package insert
バンコマイシン眼軟膏1％
PMDA Prescription drug · 東亜薬品株式会社 · package insert Dec 12, 2025
Key facts
| Brand names | バンコマイシン眼軟膏1％ |
|---|---|
| Nonproprietary names | バンコマイシン塩酸塩 |
| Companies | 製造販売元／東亜薬品株式会社, 発売元／日東メディック株式会社 |
| Product type | Prescription drug |
| Therapeutic category | グリコペプチド系抗生物質製剤 |
| Therapeutic category codes | 876113 |
| YJ codes | 6113700M1023 |
| Approval numbers | 22100AMX02256000 |
| Package insert edition | 第3版 |
| Package insert date | Dec 12, 2025 |
| PMDA document key | 480018_6113700M1023_1 |
| PMDA company code | 480018 |
At a glance
- 1–9 Package insert revisions
- 1–9 Related PMDA documents
- None Safety communications
- Yes 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: