PMDA drug package insert
KCL補正液1mEq/mL
PMDA Prescription drug · 株式会社大塚製薬工場 · package insert Oct 30, 2023
Key facts
| Brand names | KCL補正液1mEq/mL |
|---|---|
| Nonproprietary names | 塩化カリウム |
| Companies | 製造販売元／株式会社大塚製薬工場, 販売提携／大塚製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 補正用電解質液 |
| Therapeutic category codes | 873319 |
| YJ codes | 3319402A2070 |
| Approval numbers | 22000AMX00808 |
| Package insert edition | 第1版 |
| Package insert date | Oct 30, 2023 |
| PMDA document key | 180079_3319402A2070_1 |
| PMDA company code | 180079 |
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: