PMDA drug package insert
ネクセトール錠180mg
PMDA Prescription drug · 大塚製薬株式会社 · package insert Nov 12, 2025
Key facts
| Brand names | ネクセトール錠180mg |
|---|---|
| Nonproprietary names | ベムペド酸 |
| Companies | 製造販売元／大塚製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | ATPクエン酸リアーゼ阻害剤 |
| Therapeutic category codes | 872189 |
| YJ codes | 2189022F1023 |
| Approval numbers | 30700AMX00233 |
| Package insert edition | 第2版 |
| Package insert date | Nov 12, 2025 |
| PMDA document key | 180078_2189022F1023_1 |
| PMDA company code | 180078 |
At a glance
- 1–9 Package insert revisions
- 1–9 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: