PMDA drug package insert
複方ヨード・グリセリン「ニッコー」
PMDA Prescription drug · 日興製薬株式会社 · package insert Jan 22, 2024
Key facts
| Brand names | 複方ヨード・グリセリン「ニッコー」 |
|---|---|
| Nonproprietary names | 複方ヨード・グリセリン |
| Companies | 製造販売元／日興製薬株式会社, 発売元／日興製薬販売株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 口腔用剤 |
| Therapeutic category codes | 87279 |
| YJ codes | 2399700X1256 |
| Approval numbers | 16100AMZ01319 |
| Package insert edition | 第1版 |
| Package insert date | Jan 22, 2024 |
| PMDA document key | 530090_2399700X1256_2 |
| PMDA company code | 530090 |
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: