PMDA drug package insert
アナペイン注7.5mg/mL
PMDA Prescription drug · サンドファーマ株式会社 · package insert Dec 16, 2025
Key facts
| Brand names | アナペイン注7.5mg/mL, アナペイン注10mg/mL |
|---|---|
| Nonproprietary names | ロピバカイン塩酸塩水和物 |
| Companies | 製造販売／サンドファーマ株式会社, 販売／サンド株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 長時間作用性局所麻酔剤 |
| Therapeutic category codes | 871214 |
| YJ codes | 1214405A3028, 1214405A4024, 1214405A5020, 1214405A6027 |
| Approval numbers | 21300AMY00132000, 21300AMY00133000 |
| Package insert edition | 第1版 |
| Package insert date | Dec 16, 2025 |
| PMDA document key | 112268_1214405A3028_2 |
| PMDA company code | 112268 |
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: