PMDA drug package insert
ウルトラテクネカウ
PMDA Prescription drug · PDRファーマ株式会社 · package insert Apr 1, 2023
Key facts
| Brand names | ウルトラテクネカウ |
|---|---|
| Nonproprietary names | 過テクネチウム酸ナトリウム（９９ｍＴｃ）ジェネレータ |
| Companies | 製造販売元／PDRファーマ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 放射性医薬品／脳・甲状腺・唾液腺及び異所性胃粘膜疾患診断薬・局所肺換気機能診断薬 |
| Therapeutic category codes | 874300 |
| YJ codes | 4300400X1029 |
| Approval numbers | 14800AMY00047000 |
| Package insert edition | 第3版 |
| Package insert date | Apr 1, 2023 |
| PMDA document key | 651410_4300400X1029_2 |
| PMDA company code | 651410 |
At a glance
- 1–9 Package insert revisions
- 1–9 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: