PMDA drug package insert
デカドロン注射液1.65mg
PMDA Prescription drug · サンドファーマ株式会社 · package insert Apr 13, 2026
Key facts
| Brand names | デカドロン注射液1.65mg, デカドロン注射液3.3mg, デカドロン注射液6.6mg |
|---|---|
| Nonproprietary names | デキサメタゾンリン酸エステルナトリウム |
| 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 | 副腎皮質ホルモン剤 |
| Therapeutic category codes | 872454 |
| YJ codes | 2454405H1024, 2454405H3027, 2454405H5020 |
| Approval numbers | 22100AMX01399, 22100AMX01400, 22100AMX01401 |
| Package insert edition | 第6版 |
| Package insert date | Apr 13, 2026 |
| PMDA document key | 112268_2454405H1024_3 |
| PMDA company code | 112268 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- 1–9 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: