PMDA drug package insert
アマンタジン塩酸塩錠50mg「ZE」
PMDA Prescription drug · 全星薬品工業株式会社 · package insert Jul 25, 2025
Key facts
| Brand names | アマンタジン塩酸塩錠50mg「ZE」, アマンタジン塩酸塩錠100mg「ZE」 |
|---|---|
| Nonproprietary names | アマンタジン塩酸塩 |
| Companies | 製造販売元／全星薬品工業株式会社, 発売元／全星薬品株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 精神活動改善剤 パーキンソン症候群治療剤 抗A型インフルエンザウイルス剤 |
| Therapeutic category codes | 8711618711787625 |
| YJ codes | 1161001F1115, 1161001F2146 |
| Approval numbers | 22000AMX00724, 22000AMX00514 |
| Package insert edition | 第1版 |
| Package insert date | Jul 25, 2025 |
| PMDA document key | 380087_1161001F1115_1 |
| PMDA company code | 380087 |
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: