PMDA drug package insert
パラアミノ馬尿酸ソーダ注射液10%
PMDA Prescription drug · アルフレッサ ファーマ株式会社 · package insert May 26, 2026
Key facts
| Brand names | パラアミノ馬尿酸ソーダ注射液10% |
|---|---|
| Nonproprietary names | パラアミノ馬尿酸ナトリウム |
| Companies | 製造販売元／アルフレッサ ファーマ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 腎機能検査用薬 |
| Therapeutic category codes | 877225 |
| YJ codes | 7225401A1036 |
| Approval numbers | 15300AMZ00149 |
| Package insert edition | 第2版 |
| Package insert date | May 26, 2026 |
| PMDA document key | 530258_7225401A1036_1 |
| PMDA company code | 530258 |
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: