PMDA drug package insert
ダイアモックス注射用500mg
PMDA Prescription drug · 株式会社三和化学研究所 · package insert May 20, 2025
Key facts
| Brand names | ダイアモックス注射用500mg |
|---|---|
| Nonproprietary names | アセタゾラミドナトリウム |
| Companies | 製造販売元／株式会社三和化学研究所 |
| Product type | Prescription drug |
| Therapeutic category | 炭酸脱水酵素抑制剤 |
| Therapeutic category codes | 872134 |
| YJ codes | 2134400D1039 |
| Approval numbers | 21800AMX10558000 |
| Package insert edition | 第3版 |
| Package insert date | May 20, 2025 |
| PMDA document key | 300297_2134400D1039_1 |
| PMDA company code | 300297 |
At a glance
- 1–9 Package insert revisions
- 10–99 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: