PMDA drug package insert
オビソート注射用0.1g
PMDA Prescription drug · アルフレッサ ファーマ株式会社 · package insert Jun 1, 2025
Key facts
| Brand names | オビソート注射用0.1g |
|---|---|
| Nonproprietary names | 注射用アセチルコリン塩化物 |
| 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 | 自律神経剤; 循環機能検査用試薬 |
| Therapeutic category codes | 871232, 877222 |
| YJ codes | 1232400X1031 |
| Approval numbers | 22000AMX00795 |
| Package insert edition | 第2版 |
| Package insert date | Jun 1, 2025 |
| PMDA document key | 530258_1232400X1031_2 |
| PMDA company code | 530258 |
At a glance
- 1–9 Package insert revisions
- 1–9 Related PMDA documents
- None Safety communications
- Yes 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: