PMDA drug package insert
アイドロイチン1％点眼液
PMDA Prescription drug · 参天製薬株式会社 · package insert Aug 2, 2021
Key facts
| Brand names | アイドロイチン1％点眼液, アイドロイチン3％点眼液 |
|---|---|
| Nonproprietary names | コンドロイチン硫酸エステルナトリウム |
| Companies | 製造販売元／参天製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 角膜保護点眼剤 |
| Therapeutic category codes | 871319 |
| YJ codes | 1319709Q3020, 1319709Q4027 |
| Approval numbers | 14500AMZ01362, 14500AMZ01360 |
| Package insert edition | 第1版 |
| Package insert date | Aug 2, 2021 |
| PMDA document key | 300237_1319709Q3020_1 |
| PMDA company code | 300237 |
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: