PMDA drug package insert
ユニタルク胸膜腔内注入用懸濁剤4g
PMDA Prescription drug · ノーベルファーマ株式会社 · package insert Mar 29, 2022
Key facts
| Brand names | ユニタルク胸膜腔内注入用懸濁剤4g |
|---|---|
| Nonproprietary names | 滅菌調整タルク |
| Companies | 製造販売元／ノーベルファーマ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 胸膜癒着療法剤 |
| Therapeutic category codes | 874299 |
| YJ codes | 4299405D1022 |
| Approval numbers | 22500AMX01801000 |
| Package insert edition | 第1版 |
| Package insert date | Mar 29, 2022 |
| PMDA document key | 620095_4299405D1022_1 |
| PMDA company code | 620095 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- None Safety communications
- Yes PMDA review report published
- Yes 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: