PMDA drug package insert
ボースデル内用液10
PMDA Prescription drug · 健栄製薬株式会社 · package insert Jul 1, 2025
Key facts
| Brand names | ボースデル内用液10 |
|---|---|
| Nonproprietary names | 塩化マンガン四水和物 |
| Companies | 製造販売元／健栄製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | MRI用経口消化管造影剤 |
| Therapeutic category codes | 87729 |
| YJ codes | 7290006S1021 |
| Approval numbers | 21800AMZ10351000 |
| Package insert edition | 第3版 |
| Package insert date | Jul 1, 2025 |
| PMDA document key | 260024_7290006S1021_4 |
| PMDA company code | 260024 |
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: