PMDA drug package insert
強力ネオミノファーゲンシーP静注20mL
PMDA Prescription drug · 株式会社ミノファーゲン製薬 · package insert May 7, 2026
Key facts
| Brand names | 強力ネオミノファーゲンシーP静注20mL |
|---|---|
| Nonproprietary names | グリチルリチン・グリシン・システイン配合剤 |
| Companies | 製造販売元／株式会社ミノファーゲン製薬 |
| Product type | Prescription drug |
| Therapeutic category | 肝臓疾患用剤・アレルギー用薬 |
| Therapeutic category codes | 873919, 87449 |
| YJ codes | 3919502A1384 |
| Approval numbers | 22100AMX00005000 |
| Package insert edition | 第3版 |
| Package insert date | May 7, 2026 |
| PMDA document key | 750315_3919502A1384_1 |
| PMDA company code | 750315 |
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: