PMDA drug package insert
ゼジューラ錠100mg
PMDA Prescription drug · 武田薬品工業株式会社 · package insert Aug 22, 2024
Key facts
| Brand names | ゼジューラ錠100mg |
|---|---|
| Nonproprietary names | ニラパリブトシル酸塩水和物 |
| Companies | 製造販売元／武田薬品工業株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 抗悪性腫瘍剤／ポリアデノシン5'二リン酸リボースポリメラーゼ（PARP）阻害剤 |
| Therapeutic category codes | 874291 |
| YJ codes | 4291068F1028 |
| Approval numbers | 30300AMX00432 |
| Package insert edition | 第3版 |
| Package insert date | Aug 22, 2024 |
| PMDA document key | 400256_4291068F1028_1 |
| PMDA company code | 400256 |
At a glance
- 1–9 Package insert revisions
- 1–9 Related PMDA documents
- None Safety communications
- No 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: