PMDA drug package insert
ゲンタマイシン点眼液0.3％「日点」
PMDA Prescription drug · ロートニッテン株式会社 · package insert Mar 23, 2026
Key facts
| Brand names | ゲンタマイシン点眼液0.3％「日点」 |
|---|---|
| Nonproprietary names | ゲンタマイシン硫酸塩 |
| Companies | 製造販売元／ロートニッテン株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 眼科用抗生物質製剤 |
| Therapeutic category codes | 871317 |
| YJ codes | 1317706Q1119 |
| Approval numbers | 23000AMX00592000 |
| Package insert edition | 第2版 |
| Package insert date | Mar 23, 2026 |
| PMDA document key | 530304_1317706Q1119_1 |
| PMDA company code | 530304 |
At a glance
- 1–9 Package insert revisions
- 1–9 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: