PMDA drug package insert
イオヘキソール300注20mL「F」
PMDA Prescription drug · 富士製薬工業株式会社 · package insert Oct 9, 2024
Key facts
| Brand names | イオヘキソール300注20mL「F」, イオヘキソール300注50mL「F」, イオヘキソール300注100mL「F」, イオヘキソール350注20mL「F」, イオヘキソール350注50mL「F」, イオヘキソール350注100mL「F」 |
|---|---|
| Nonproprietary names | イオヘキソール |
| Companies | 製造販売元(輸入)／富士製薬工業株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 非イオン性造影剤 |
| Therapeutic category codes | 877219 |
| YJ codes | 7219415A9090, 7219415H1101, 7219415H2108, 7219415H3082, 7219415H4089, 7219415H5085 |
| Approval numbers | 30200AMX00645, 30200AMX00646, 30200AMX00647, 30200AMX00648, 30200AMX00649, 30200AMX00650 |
| Package insert edition | 第2版 |
| Package insert date | Oct 9, 2024 |
| PMDA document key | 670109_7219415A9090_1 |
| PMDA company code | 670109 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- None 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: