PMDA drug package insert
スルピリド錠50mg「アメル」
PMDA Prescription drug · 共和薬品工業株式会社 · package insert May 20, 2025
Key facts
| Brand names | スルピリド錠50mg「アメル」 |
|---|---|
| Nonproprietary names | スルピリド |
| Companies | 製造販売元／共和薬品工業株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 精神情動安定剤; 視床下部作用性抗潰瘍剤 |
| Therapeutic category codes | 871179, 872329 |
| YJ codes | 2329009F1152 |
| Approval numbers | 21700AMZ00358 |
| Package insert edition | 第3版 |
| Package insert date | May 20, 2025 |
| PMDA document key | 672173_2329009F1152_1 |
| PMDA company code | 672173 |
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: