PMDA drug package insert
歯科用TDゼット・ゼリー
PMDA Prescription drug · 東洋製薬化成株式会社 · package insert May 10, 2023
Key facts
| Brand names | 歯科用TDゼット・ゼリー |
|---|---|
| Nonproprietary names | 塩化アルミニウム・セチルピリジニウム配合剤 |
| 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 | 口腔内局所止血剤 |
| Therapeutic category codes | 87279 |
| YJ codes | 2790821P1023 |
| Approval numbers | 16100AMZ03444 |
| Package insert edition | 第1版 |
| Package insert date | May 10, 2023 |
| PMDA document key | 480199_2790821P1023_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: