PMDA drug package insert
ウゴービ皮下注0.25mgペン 1.0MD
PMDA Prescription drug · ノボ ノルディスク ファーマ株式会社 · package insert Jun 19, 2026
Key facts
| Brand names | ウゴービ皮下注0.25mgペン 1.0MD, ウゴービ皮下注0.5mgペン 2.0MD, ウゴービ皮下注1.0mgペン 4.0MD, ウゴービ皮下注1.7mgペン 6.8MD, ウゴービ皮下注2.4mgペン 9.6MD |
|---|---|
| Nonproprietary names | セマグルチド（遺伝子組換え） |
| Companies | 製造販売元／ノボ ノルディスク ファーマ株式会社, プロモーション提携／住友ファーマ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 肥満症・MASH治療剤 持続性GLP-1受容体作動薬 |
| Therapeutic category codes | 872499 |
| YJ codes | 2499418P1028, 2499418P2024, 2499418P3020, 2499418P4027, 2499418P5023 |
| Approval numbers | 30700AMX00001000, 30700AMX00002000, 30700AMX00003000, 30700AMX00004000, 30700AMX00005000 |
| Package insert edition | 第5版 |
| Package insert date | Jun 19, 2026 |
| PMDA document key | 620023_2499418P1028_1 |
| PMDA company code | 620023 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- None Safety communications
- Yes PMDA review report published
- Yes 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: