PMDA drug package insert
サホライド液歯科用38%
PMDA Prescription drug · 東洋製薬化成株式会社 · package insert Jul 12, 2023
Key facts
| Brand names | サホライド液歯科用38% |
|---|---|
| Nonproprietary names | フッ化ジアンミン銀 |
| Companies | 製造販売元／東洋製薬化成株式会社, 発売元／株式会社ビーブランド・メディコーデンタル |
| Product type | Prescription drug |
| Therapeutic category | う蝕抑制・象牙質知覚過敏鈍麻剤 |
| Therapeutic category codes | 87279 |
| YJ codes | 2790802Q1034 |
| Approval numbers | 22100AMX00451 |
| Package insert edition | 第1版 |
| Package insert date | Jul 12, 2023 |
| PMDA document key | 480199_2790802Q1034_1 |
| PMDA company code | 480199 |
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: