PMDA drug package insert
カーディオライト 第一
PMDA Prescription drug · PDRファーマ株式会社 · package insert Jun 1, 2026
Key facts
| Brand names | カーディオライト 第一 |
|---|---|
| Nonproprietary names | テトラキスメトキシイソブチルイソニトリル銅（Ｉ）四フッ化ホウ酸 |
| Companies | 製造販売元／PDRファーマ株式会社, 輸入先／SHINE SPECT USA, LLC（米国） |
| Product type | Prescription drug |
| Therapeutic category | 放射性医薬品／心臓疾患診断薬・心機能診断薬・副甲状腺疾患診断薬 |
| Therapeutic category codes | 874300 |
| YJ codes | 4300439D1024 |
| Approval numbers | 20500AMY00127000 |
| Package insert edition | 第3版 |
| Package insert date | Jun 1, 2026 |
| PMDA document key | 651410_4300439D1024_2 |
| PMDA company code | 651410 |
At a glance
- 1–9 Package insert revisions
- 1–9 Related PMDA documents
- 1–9 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: