PMDA drug package insert
ドブトレックスキット点滴静注用200mg
PMDA Prescription drug · 共和薬品工業株式会社 · package insert Mar 30, 2026
Key facts
| Brand names | ドブトレックスキット点滴静注用200mg, ドブトレックスキット点滴静注用600mg |
|---|---|
| Nonproprietary names | ドブタミン塩酸塩 |
| Companies | 製造販売元／共和薬品工業株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 急性循環不全改善剤; 心臓疾患診断補助剤 |
| Therapeutic category codes | 872119, 87799 |
| YJ codes | 2119404G3056, 2119404G4052 |
| Approval numbers | 21900AMX00719, 21900AMX00720 |
| Package insert edition | 第2版 |
| Package insert date | Mar 30, 2026 |
| PMDA document key | 672173_2119404G3056_3 |
| PMDA company code | 672173 |
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: