PMDA drug package insert
メンドンカプセル7.5mg
PMDA Prescription drug · ヴィアトリス製薬合同会社 · package insert Jul 1, 2024
Key facts
| Brand names | メンドンカプセル7.5mg |
|---|---|
| Nonproprietary names | クロラゼプ酸二カリウム |
| Companies | 製造販売元／ヴィアトリス製薬合同会社 |
| Product type | Prescription drug |
| Therapeutic category | 抗不安剤 |
| Therapeutic category codes | 871124 |
| YJ codes | 1124015M2038 |
| Approval numbers | 22100AMX01338 |
| Package insert edition | 第4版 |
| Package insert date | Jul 1, 2024 |
| PMDA document key | 671450_1124015M2038_3 |
| PMDA company code | 671450 |
At a glance
- 1–9 Package insert revisions
- 1–9 Related PMDA documents
- 1–9 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: