PMDA drug package insert
KCL注10mEqキット「テルモ」
PMDA Prescription drug · テルモ株式会社 · package insert Apr 10, 2023
Key facts
| Brand names | KCL注10mEqキット「テルモ」, KCL注20mEqキット「テルモ」 |
|---|---|
| Nonproprietary names | 塩化カリウム |
| Companies | 製造販売元／テルモ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 補正用電解質液 |
| Therapeutic category codes | 873319 |
| YJ codes | 3319402G3028, 3319402G4024 |
| Approval numbers | 21800AMX10627, 21800AMX10628 |
| Package insert edition | 第1版 |
| Package insert date | Apr 10, 2023 |
| PMDA document key | 470034_3319402G3028_1 |
| PMDA company code | 470034 |
At a glance
- 1–9 Package insert revisions
- 1–9 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: