PMDA drug package insert
グルカゴンGノボ注射用1mg（添付溶解液あり）
PMDA Prescription drug · ノボ ノルディスク ファーマ株式会社 溶解液 · package insert Jan 23, 2026
Key facts
| Brand names | グルカゴンGノボ注射用1mg（添付溶解液あり） |
|---|---|
| Nonproprietary names | グルカゴン（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 溶解液, 製造販売元／光製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | グルカゴン（遺伝子組換え) |
| Therapeutic category codes | 872492, 87722 |
| YJ codes | 7229402D1036 |
| Approval numbers | 22100AMX01356000 |
| Package insert edition | 第2版 |
| Package insert date | Jan 23, 2026 |
| PMDA document key | 620023_7229402D1036_1 |
| PMDA company code | 620023 |
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: