PMDA drug package insert
人工涙液マイティア点眼液
PMDA Prescription drug · 千寿製薬株式会社 · package insert Aug 3, 2026
Key facts
| Brand names | 人工涙液マイティア点眼液 |
|---|---|
| Nonproprietary names | ホウ酸・無機塩類配合剤 |
| Companies | 製造販売元／千寿製薬株式会社, 販売／武田薬品工業株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 点眼液 |
| Therapeutic category codes | 871319 |
| YJ codes | 1319808Q2036 |
| Approval numbers | 21800AMX10532 |
| Package insert edition | 第2版 |
| Package insert date | Aug 3, 2026 |
| PMDA document key | 380086_1319808Q2036_1 |
| PMDA company code | 380086 |
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: